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NM_007294.4(BRCA1):c.4636G>A (p.Asp1546Asn) AND not specified

Germline classification:
Benign/Likely benign (6 submissions)
Last evaluated:
Aug 15, 2023
Review status:
2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000123923.28

Allele description [Variation Report for NM_007294.4(BRCA1):c.4636G>A (p.Asp1546Asn)]

NM_007294.4(BRCA1):c.4636G>A (p.Asp1546Asn)

Gene:
BRCA1:BRCA1 DNA repair associated [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
17q21.31
Genomic location:
Preferred name:
NM_007294.4(BRCA1):c.4636G>A (p.Asp1546Asn)
Other names:
p.D1546N:GAT>AAT; 4755G>A; NP_009225.1:p.Asp1546Asn
HGVS:
  • NC_000017.11:g.43074370C>T
  • NG_005905.2:g.143614G>A
  • NM_001407571.1:c.4423G>A
  • NM_001407581.1:c.4702G>A
  • NM_001407582.1:c.4702G>A
  • NM_001407583.1:c.4699G>A
  • NM_001407585.1:c.4699G>A
  • NM_001407587.1:c.4699G>A
  • NM_001407590.1:c.4696G>A
  • NM_001407591.1:c.4696G>A
  • NM_001407593.1:c.4636G>A
  • NM_001407594.1:c.4636G>A
  • NM_001407596.1:c.4636G>A
  • NM_001407597.1:c.4636G>A
  • NM_001407598.1:c.4636G>A
  • NM_001407602.1:c.4636G>A
  • NM_001407603.1:c.4636G>A
  • NM_001407605.1:c.4636G>A
  • NM_001407610.1:c.4633G>A
  • NM_001407611.1:c.4633G>A
  • NM_001407612.1:c.4633G>A
  • NM_001407613.1:c.4633G>A
  • NM_001407614.1:c.4633G>A
  • NM_001407615.1:c.4633G>A
  • NM_001407616.1:c.4633G>A
  • NM_001407617.1:c.4633G>A
  • NM_001407618.1:c.4633G>A
  • NM_001407619.1:c.4633G>A
  • NM_001407620.1:c.4633G>A
  • NM_001407621.1:c.4633G>A
  • NM_001407622.1:c.4633G>A
  • NM_001407623.1:c.4633G>A
  • NM_001407624.1:c.4633G>A
  • NM_001407625.1:c.4633G>A
  • NM_001407626.1:c.4633G>A
  • NM_001407627.1:c.4630G>A
  • NM_001407628.1:c.4630G>A
  • NM_001407629.1:c.4630G>A
  • NM_001407630.1:c.4630G>A
  • NM_001407631.1:c.4630G>A
  • NM_001407632.1:c.4630G>A
  • NM_001407633.1:c.4630G>A
  • NM_001407634.1:c.4630G>A
  • NM_001407635.1:c.4630G>A
  • NM_001407636.1:c.4630G>A
  • NM_001407637.1:c.4630G>A
  • NM_001407638.1:c.4630G>A
  • NM_001407639.1:c.4630G>A
  • NM_001407640.1:c.4630G>A
  • NM_001407641.1:c.4630G>A
  • NM_001407642.1:c.4630G>A
  • NM_001407644.1:c.4627G>A
  • NM_001407645.1:c.4627G>A
  • NM_001407646.1:c.4624G>A
  • NM_001407647.1:c.4621G>A
  • NM_001407648.1:c.4579G>A
  • NM_001407649.1:c.4576G>A
  • NM_001407652.1:c.4636G>A
  • NM_001407653.1:c.4558G>A
  • NM_001407654.1:c.4558G>A
  • NM_001407655.1:c.4558G>A
  • NM_001407656.1:c.4555G>A
  • NM_001407657.1:c.4555G>A
  • NM_001407658.1:c.4555G>A
  • NM_001407659.1:c.4552G>A
  • NM_001407660.1:c.4552G>A
  • NM_001407661.1:c.4552G>A
  • NM_001407662.1:c.4552G>A
  • NM_001407663.1:c.4552G>A
  • NM_001407664.1:c.4513G>A
  • NM_001407665.1:c.4513G>A
  • NM_001407666.1:c.4513G>A
  • NM_001407667.1:c.4513G>A
  • NM_001407668.1:c.4513G>A
  • NM_001407669.1:c.4513G>A
  • NM_001407670.1:c.4510G>A
  • NM_001407671.1:c.4510G>A
  • NM_001407672.1:c.4510G>A
  • NM_001407673.1:c.4510G>A
  • NM_001407674.1:c.4510G>A
  • NM_001407675.1:c.4510G>A
  • NM_001407676.1:c.4510G>A
  • NM_001407677.1:c.4510G>A
  • NM_001407678.1:c.4510G>A
  • NM_001407679.1:c.4510G>A
  • NM_001407680.1:c.4510G>A
  • NM_001407681.1:c.4507G>A
  • NM_001407682.1:c.4507G>A
  • NM_001407683.1:c.4507G>A
  • NM_001407684.1:c.4636G>A
  • NM_001407685.1:c.4507G>A
  • NM_001407686.1:c.4507G>A
  • NM_001407687.1:c.4507G>A
  • NM_001407688.1:c.4507G>A
  • NM_001407689.1:c.4507G>A
  • NM_001407690.1:c.4504G>A
  • NM_001407691.1:c.4504G>A
  • NM_001407692.1:c.4495G>A
  • NM_001407694.1:c.4495G>A
  • NM_001407695.1:c.4495G>A
  • NM_001407696.1:c.4495G>A
  • NM_001407697.1:c.4495G>A
  • NM_001407698.1:c.4495G>A
  • NM_001407724.1:c.4495G>A
  • NM_001407725.1:c.4495G>A
  • NM_001407726.1:c.4495G>A
  • NM_001407727.1:c.4495G>A
  • NM_001407728.1:c.4495G>A
  • NM_001407729.1:c.4495G>A
  • NM_001407730.1:c.4495G>A
  • NM_001407731.1:c.4495G>A
  • NM_001407732.1:c.4492G>A
  • NM_001407733.1:c.4492G>A
  • NM_001407734.1:c.4492G>A
  • NM_001407735.1:c.4492G>A
  • NM_001407736.1:c.4492G>A
  • NM_001407737.1:c.4492G>A
  • NM_001407738.1:c.4492G>A
  • NM_001407739.1:c.4492G>A
  • NM_001407740.1:c.4492G>A
  • NM_001407741.1:c.4492G>A
  • NM_001407742.1:c.4492G>A
  • NM_001407743.1:c.4492G>A
  • NM_001407744.1:c.4492G>A
  • NM_001407745.1:c.4492G>A
  • NM_001407746.1:c.4492G>A
  • NM_001407747.1:c.4492G>A
  • NM_001407748.1:c.4492G>A
  • NM_001407749.1:c.4492G>A
  • NM_001407750.1:c.4492G>A
  • NM_001407751.1:c.4492G>A
  • NM_001407752.1:c.4492G>A
  • NM_001407838.1:c.4489G>A
  • NM_001407839.1:c.4489G>A
  • NM_001407841.1:c.4489G>A
  • NM_001407842.1:c.4489G>A
  • NM_001407843.1:c.4489G>A
  • NM_001407844.1:c.4489G>A
  • NM_001407845.1:c.4489G>A
  • NM_001407846.1:c.4489G>A
  • NM_001407847.1:c.4489G>A
  • NM_001407848.1:c.4489G>A
  • NM_001407849.1:c.4489G>A
  • NM_001407850.1:c.4489G>A
  • NM_001407851.1:c.4489G>A
  • NM_001407852.1:c.4489G>A
  • NM_001407853.1:c.4489G>A
  • NM_001407854.1:c.4636G>A
  • NM_001407858.1:c.4633G>A
  • NM_001407859.1:c.4633G>A
  • NM_001407860.1:c.4633G>A
  • NM_001407861.1:c.4630G>A
  • NM_001407862.1:c.4435G>A
  • NM_001407863.1:c.4510G>A
  • NM_001407874.1:c.4429G>A
  • NM_001407875.1:c.4429G>A
  • NM_001407879.1:c.4426G>A
  • NM_001407881.1:c.4426G>A
  • NM_001407882.1:c.4426G>A
  • NM_001407884.1:c.4426G>A
  • NM_001407885.1:c.4426G>A
  • NM_001407886.1:c.4426G>A
  • NM_001407887.1:c.4426G>A
  • NM_001407889.1:c.4426G>A
  • NM_001407894.1:c.4423G>A
  • NM_001407895.1:c.4423G>A
  • NM_001407896.1:c.4423G>A
  • NM_001407897.1:c.4423G>A
  • NM_001407898.1:c.4423G>A
  • NM_001407899.1:c.4423G>A
  • NM_001407900.1:c.4423G>A
  • NM_001407902.1:c.4423G>A
  • NM_001407904.1:c.4423G>A
  • NM_001407906.1:c.4423G>A
  • NM_001407907.1:c.4423G>A
  • NM_001407908.1:c.4423G>A
  • NM_001407909.1:c.4423G>A
  • NM_001407910.1:c.4423G>A
  • NM_001407915.1:c.4420G>A
  • NM_001407916.1:c.4420G>A
  • NM_001407917.1:c.4420G>A
  • NM_001407918.1:c.4420G>A
  • NM_001407919.1:c.4513G>A
  • NM_001407920.1:c.4372G>A
  • NM_001407921.1:c.4372G>A
  • NM_001407922.1:c.4372G>A
  • NM_001407923.1:c.4372G>A
  • NM_001407924.1:c.4372G>A
  • NM_001407925.1:c.4372G>A
  • NM_001407926.1:c.4372G>A
  • NM_001407927.1:c.4369G>A
  • NM_001407928.1:c.4369G>A
  • NM_001407929.1:c.4369G>A
  • NM_001407930.1:c.4369G>A
  • NM_001407931.1:c.4369G>A
  • NM_001407932.1:c.4369G>A
  • NM_001407933.1:c.4369G>A
  • NM_001407934.1:c.4366G>A
  • NM_001407935.1:c.4366G>A
  • NM_001407936.1:c.4366G>A
  • NM_001407937.1:c.4513G>A
  • NM_001407938.1:c.4513G>A
  • NM_001407939.1:c.4510G>A
  • NM_001407940.1:c.4510G>A
  • NM_001407941.1:c.4507G>A
  • NM_001407942.1:c.4495G>A
  • NM_001407943.1:c.4492G>A
  • NM_001407944.1:c.4492G>A
  • NM_001407945.1:c.4492G>A
  • NM_001407946.1:c.4303G>A
  • NM_001407947.1:c.4303G>A
  • NM_001407948.1:c.4303G>A
  • NM_001407949.1:c.4303G>A
  • NM_001407950.1:c.4300G>A
  • NM_001407951.1:c.4300G>A
  • NM_001407952.1:c.4300G>A
  • NM_001407953.1:c.4300G>A
  • NM_001407954.1:c.4300G>A
  • NM_001407955.1:c.4300G>A
  • NM_001407956.1:c.4297G>A
  • NM_001407957.1:c.4297G>A
  • NM_001407958.1:c.4297G>A
  • NM_001407959.1:c.4255G>A
  • NM_001407960.1:c.4252G>A
  • NM_001407962.1:c.4252G>A
  • NM_001407963.1:c.4249G>A
  • NM_001407965.1:c.4129G>A
  • NM_001407966.1:c.3748G>A
  • NM_001407967.1:c.3745G>A
  • NM_001407968.1:c.2032G>A
  • NM_001407969.1:c.2029G>A
  • NM_001407970.1:c.1393G>A
  • NM_001407971.1:c.1393G>A
  • NM_001407972.1:c.1390G>A
  • NM_001407973.1:c.1327G>A
  • NM_001407974.1:c.1327G>A
  • NM_001407975.1:c.1327G>A
  • NM_001407976.1:c.1327G>A
  • NM_001407977.1:c.1327G>A
  • NM_001407978.1:c.1327G>A
  • NM_001407979.1:c.1324G>A
  • NM_001407980.1:c.1324G>A
  • NM_001407981.1:c.1324G>A
  • NM_001407982.1:c.1324G>A
  • NM_001407983.1:c.1324G>A
  • NM_001407984.1:c.1324G>A
  • NM_001407985.1:c.1324G>A
  • NM_001407986.1:c.1324G>A
  • NM_001407990.1:c.1324G>A
  • NM_001407991.1:c.1324G>A
  • NM_001407992.1:c.1324G>A
  • NM_001407993.1:c.1324G>A
  • NM_001408392.1:c.1321G>A
  • NM_001408396.1:c.1321G>A
  • NM_001408397.1:c.1321G>A
  • NM_001408398.1:c.1321G>A
  • NM_001408399.1:c.1321G>A
  • NM_001408400.1:c.1321G>A
  • NM_001408401.1:c.1321G>A
  • NM_001408402.1:c.1321G>A
  • NM_001408403.1:c.1321G>A
  • NM_001408404.1:c.1321G>A
  • NM_001408406.1:c.1318G>A
  • NM_001408407.1:c.1318G>A
  • NM_001408408.1:c.1318G>A
  • NM_001408409.1:c.1315G>A
  • NM_001408410.1:c.1252G>A
  • NM_001408411.1:c.1249G>A
  • NM_001408412.1:c.1246G>A
  • NM_001408413.1:c.1246G>A
  • NM_001408414.1:c.1246G>A
  • NM_001408415.1:c.1246G>A
  • NM_001408416.1:c.1246G>A
  • NM_001408418.1:c.1210G>A
  • NM_001408419.1:c.1210G>A
  • NM_001408420.1:c.1210G>A
  • NM_001408421.1:c.1207G>A
  • NM_001408422.1:c.1207G>A
  • NM_001408423.1:c.1207G>A
  • NM_001408424.1:c.1207G>A
  • NM_001408425.1:c.1204G>A
  • NM_001408426.1:c.1204G>A
  • NM_001408427.1:c.1204G>A
  • NM_001408428.1:c.1204G>A
  • NM_001408429.1:c.1204G>A
  • NM_001408430.1:c.1204G>A
  • NM_001408431.1:c.1204G>A
  • NM_001408432.1:c.1201G>A
  • NM_001408433.1:c.1201G>A
  • NM_001408434.1:c.1201G>A
  • NM_001408435.1:c.1201G>A
  • NM_001408436.1:c.1201G>A
  • NM_001408437.1:c.1201G>A
  • NM_001408438.1:c.1201G>A
  • NM_001408439.1:c.1201G>A
  • NM_001408440.1:c.1201G>A
  • NM_001408441.1:c.1201G>A
  • NM_001408442.1:c.1201G>A
  • NM_001408443.1:c.1201G>A
  • NM_001408444.1:c.1201G>A
  • NM_001408445.1:c.1198G>A
  • NM_001408446.1:c.1198G>A
  • NM_001408447.1:c.1198G>A
  • NM_001408448.1:c.1198G>A
  • NM_001408450.1:c.1198G>A
  • NM_001408451.1:c.1192G>A
  • NM_001408452.1:c.1186G>A
  • NM_001408453.1:c.1186G>A
  • NM_001408454.1:c.1186G>A
  • NM_001408455.1:c.1186G>A
  • NM_001408456.1:c.1186G>A
  • NM_001408457.1:c.1186G>A
  • NM_001408458.1:c.1183G>A
  • NM_001408459.1:c.1183G>A
  • NM_001408460.1:c.1183G>A
  • NM_001408461.1:c.1183G>A
  • NM_001408462.1:c.1183G>A
  • NM_001408463.1:c.1183G>A
  • NM_001408464.1:c.1183G>A
  • NM_001408465.1:c.1183G>A
  • NM_001408466.1:c.1183G>A
  • NM_001408467.1:c.1183G>A
  • NM_001408468.1:c.1180G>A
  • NM_001408469.1:c.1180G>A
  • NM_001408470.1:c.1180G>A
  • NM_001408472.1:c.1324G>A
  • NM_001408473.1:c.1321G>A
  • NM_001408474.1:c.1126G>A
  • NM_001408475.1:c.1123G>A
  • NM_001408476.1:c.1123G>A
  • NM_001408478.1:c.1117G>A
  • NM_001408479.1:c.1117G>A
  • NM_001408480.1:c.1117G>A
  • NM_001408481.1:c.1114G>A
  • NM_001408482.1:c.1114G>A
  • NM_001408483.1:c.1114G>A
  • NM_001408484.1:c.1114G>A
  • NM_001408485.1:c.1114G>A
  • NM_001408489.1:c.1114G>A
  • NM_001408490.1:c.1114G>A
  • NM_001408491.1:c.1114G>A
  • NM_001408492.1:c.1111G>A
  • NM_001408493.1:c.1111G>A
  • NM_001408494.1:c.1087G>A
  • NM_001408495.1:c.1081G>A
  • NM_001408496.1:c.1063G>A
  • NM_001408497.1:c.1063G>A
  • NM_001408498.1:c.1063G>A
  • NM_001408499.1:c.1063G>A
  • NM_001408500.1:c.1063G>A
  • NM_001408501.1:c.1063G>A
  • NM_001408502.1:c.1060G>A
  • NM_001408503.1:c.1060G>A
  • NM_001408504.1:c.1060G>A
  • NM_001408505.1:c.1057G>A
  • NM_001408506.1:c.1000G>A
  • NM_001408507.1:c.997G>A
  • NM_001408508.1:c.988G>A
  • NM_001408509.1:c.985G>A
  • NM_001408510.1:c.946G>A
  • NM_001408511.1:c.943G>A
  • NM_001408512.1:c.823G>A
  • NM_007294.4:c.4636G>AMANE SELECT
  • NM_007297.4:c.4495G>A
  • NM_007298.4:c.1324G>A
  • NM_007299.4:c.1324G>A
  • NM_007300.4:c.4699G>A
  • NM_007304.2:c.1324G>A
  • NP_001394500.1:p.Asp1475Asn
  • NP_001394510.1:p.Asp1568Asn
  • NP_001394511.1:p.Asp1568Asn
  • NP_001394512.1:p.Asp1567Asn
  • NP_001394514.1:p.Asp1567Asn
  • NP_001394516.1:p.Asp1567Asn
  • NP_001394519.1:p.Asp1566Asn
  • NP_001394520.1:p.Asp1566Asn
  • NP_001394522.1:p.Asp1546Asn
  • NP_001394523.1:p.Asp1546Asn
  • NP_001394525.1:p.Asp1546Asn
  • NP_001394526.1:p.Asp1546Asn
  • NP_001394527.1:p.Asp1546Asn
  • NP_001394531.1:p.Asp1546Asn
  • NP_001394532.1:p.Asp1546Asn
  • NP_001394534.1:p.Asp1546Asn
  • NP_001394539.1:p.Asp1545Asn
  • NP_001394540.1:p.Asp1545Asn
  • NP_001394541.1:p.Asp1545Asn
  • NP_001394542.1:p.Asp1545Asn
  • NP_001394543.1:p.Asp1545Asn
  • NP_001394544.1:p.Asp1545Asn
  • NP_001394545.1:p.Asp1545Asn
  • NP_001394546.1:p.Asp1545Asn
  • NP_001394547.1:p.Asp1545Asn
  • NP_001394548.1:p.Asp1545Asn
  • NP_001394549.1:p.Asp1545Asn
  • NP_001394550.1:p.Asp1545Asn
  • NP_001394551.1:p.Asp1545Asn
  • NP_001394552.1:p.Asp1545Asn
  • NP_001394553.1:p.Asp1545Asn
  • NP_001394554.1:p.Asp1545Asn
  • NP_001394555.1:p.Asp1545Asn
  • NP_001394556.1:p.Asp1544Asn
  • NP_001394557.1:p.Asp1544Asn
  • NP_001394558.1:p.Asp1544Asn
  • NP_001394559.1:p.Asp1544Asn
  • NP_001394560.1:p.Asp1544Asn
  • NP_001394561.1:p.Asp1544Asn
  • NP_001394562.1:p.Asp1544Asn
  • NP_001394563.1:p.Asp1544Asn
  • NP_001394564.1:p.Asp1544Asn
  • NP_001394565.1:p.Asp1544Asn
  • NP_001394566.1:p.Asp1544Asn
  • NP_001394567.1:p.Asp1544Asn
  • NP_001394568.1:p.Asp1544Asn
  • NP_001394569.1:p.Asp1544Asn
  • NP_001394570.1:p.Asp1544Asn
  • NP_001394571.1:p.Asp1544Asn
  • NP_001394573.1:p.Asp1543Asn
  • NP_001394574.1:p.Asp1543Asn
  • NP_001394575.1:p.Asp1542Asn
  • NP_001394576.1:p.Asp1541Asn
  • NP_001394577.1:p.Asp1527Asn
  • NP_001394578.1:p.Asp1526Asn
  • NP_001394581.1:p.Asp1546Asn
  • NP_001394582.1:p.Asp1520Asn
  • NP_001394583.1:p.Asp1520Asn
  • NP_001394584.1:p.Asp1520Asn
  • NP_001394585.1:p.Asp1519Asn
  • NP_001394586.1:p.Asp1519Asn
  • NP_001394587.1:p.Asp1519Asn
  • NP_001394588.1:p.Asp1518Asn
  • NP_001394589.1:p.Asp1518Asn
  • NP_001394590.1:p.Asp1518Asn
  • NP_001394591.1:p.Asp1518Asn
  • NP_001394592.1:p.Asp1518Asn
  • NP_001394593.1:p.Asp1505Asn
  • NP_001394594.1:p.Asp1505Asn
  • NP_001394595.1:p.Asp1505Asn
  • NP_001394596.1:p.Asp1505Asn
  • NP_001394597.1:p.Asp1505Asn
  • NP_001394598.1:p.Asp1505Asn
  • NP_001394599.1:p.Asp1504Asn
  • NP_001394600.1:p.Asp1504Asn
  • NP_001394601.1:p.Asp1504Asn
  • NP_001394602.1:p.Asp1504Asn
  • NP_001394603.1:p.Asp1504Asn
  • NP_001394604.1:p.Asp1504Asn
  • NP_001394605.1:p.Asp1504Asn
  • NP_001394606.1:p.Asp1504Asn
  • NP_001394607.1:p.Asp1504Asn
  • NP_001394608.1:p.Asp1504Asn
  • NP_001394609.1:p.Asp1504Asn
  • NP_001394610.1:p.Asp1503Asn
  • NP_001394611.1:p.Asp1503Asn
  • NP_001394612.1:p.Asp1503Asn
  • NP_001394613.1:p.Asp1546Asn
  • NP_001394614.1:p.Asp1503Asn
  • NP_001394615.1:p.Asp1503Asn
  • NP_001394616.1:p.Asp1503Asn
  • NP_001394617.1:p.Asp1503Asn
  • NP_001394618.1:p.Asp1503Asn
  • NP_001394619.1:p.Asp1502Asn
  • NP_001394620.1:p.Asp1502Asn
  • NP_001394621.1:p.Asp1499Asn
  • NP_001394623.1:p.Asp1499Asn
  • NP_001394624.1:p.Asp1499Asn
  • NP_001394625.1:p.Asp1499Asn
  • NP_001394626.1:p.Asp1499Asn
  • NP_001394627.1:p.Asp1499Asn
  • NP_001394653.1:p.Asp1499Asn
  • NP_001394654.1:p.Asp1499Asn
  • NP_001394655.1:p.Asp1499Asn
  • NP_001394656.1:p.Asp1499Asn
  • NP_001394657.1:p.Asp1499Asn
  • NP_001394658.1:p.Asp1499Asn
  • NP_001394659.1:p.Asp1499Asn
  • NP_001394660.1:p.Asp1499Asn
  • NP_001394661.1:p.Asp1498Asn
  • NP_001394662.1:p.Asp1498Asn
  • NP_001394663.1:p.Asp1498Asn
  • NP_001394664.1:p.Asp1498Asn
  • NP_001394665.1:p.Asp1498Asn
  • NP_001394666.1:p.Asp1498Asn
  • NP_001394667.1:p.Asp1498Asn
  • NP_001394668.1:p.Asp1498Asn
  • NP_001394669.1:p.Asp1498Asn
  • NP_001394670.1:p.Asp1498Asn
  • NP_001394671.1:p.Asp1498Asn
  • NP_001394672.1:p.Asp1498Asn
  • NP_001394673.1:p.Asp1498Asn
  • NP_001394674.1:p.Asp1498Asn
  • NP_001394675.1:p.Asp1498Asn
  • NP_001394676.1:p.Asp1498Asn
  • NP_001394677.1:p.Asp1498Asn
  • NP_001394678.1:p.Asp1498Asn
  • NP_001394679.1:p.Asp1498Asn
  • NP_001394680.1:p.Asp1498Asn
  • NP_001394681.1:p.Asp1498Asn
  • NP_001394767.1:p.Asp1497Asn
  • NP_001394768.1:p.Asp1497Asn
  • NP_001394770.1:p.Asp1497Asn
  • NP_001394771.1:p.Asp1497Asn
  • NP_001394772.1:p.Asp1497Asn
  • NP_001394773.1:p.Asp1497Asn
  • NP_001394774.1:p.Asp1497Asn
  • NP_001394775.1:p.Asp1497Asn
  • NP_001394776.1:p.Asp1497Asn
  • NP_001394777.1:p.Asp1497Asn
  • NP_001394778.1:p.Asp1497Asn
  • NP_001394779.1:p.Asp1497Asn
  • NP_001394780.1:p.Asp1497Asn
  • NP_001394781.1:p.Asp1497Asn
  • NP_001394782.1:p.Asp1497Asn
  • NP_001394783.1:p.Asp1546Asn
  • NP_001394787.1:p.Asp1545Asn
  • NP_001394788.1:p.Asp1545Asn
  • NP_001394789.1:p.Asp1545Asn
  • NP_001394790.1:p.Asp1544Asn
  • NP_001394791.1:p.Asp1479Asn
  • NP_001394792.1:p.Asp1504Asn
  • NP_001394803.1:p.Asp1477Asn
  • NP_001394804.1:p.Asp1477Asn
  • NP_001394808.1:p.Asp1476Asn
  • NP_001394810.1:p.Asp1476Asn
  • NP_001394811.1:p.Asp1476Asn
  • NP_001394813.1:p.Asp1476Asn
  • NP_001394814.1:p.Asp1476Asn
  • NP_001394815.1:p.Asp1476Asn
  • NP_001394816.1:p.Asp1476Asn
  • NP_001394818.1:p.Asp1476Asn
  • NP_001394823.1:p.Asp1475Asn
  • NP_001394824.1:p.Asp1475Asn
  • NP_001394825.1:p.Asp1475Asn
  • NP_001394826.1:p.Asp1475Asn
  • NP_001394827.1:p.Asp1475Asn
  • NP_001394828.1:p.Asp1475Asn
  • NP_001394829.1:p.Asp1475Asn
  • NP_001394831.1:p.Asp1475Asn
  • NP_001394833.1:p.Asp1475Asn
  • NP_001394835.1:p.Asp1475Asn
  • NP_001394836.1:p.Asp1475Asn
  • NP_001394837.1:p.Asp1475Asn
  • NP_001394838.1:p.Asp1475Asn
  • NP_001394839.1:p.Asp1475Asn
  • NP_001394844.1:p.Asp1474Asn
  • NP_001394845.1:p.Asp1474Asn
  • NP_001394846.1:p.Asp1474Asn
  • NP_001394847.1:p.Asp1474Asn
  • NP_001394848.1:p.Asp1505Asn
  • NP_001394849.1:p.Asp1458Asn
  • NP_001394850.1:p.Asp1458Asn
  • NP_001394851.1:p.Asp1458Asn
  • NP_001394852.1:p.Asp1458Asn
  • NP_001394853.1:p.Asp1458Asn
  • NP_001394854.1:p.Asp1458Asn
  • NP_001394855.1:p.Asp1458Asn
  • NP_001394856.1:p.Asp1457Asn
  • NP_001394857.1:p.Asp1457Asn
  • NP_001394858.1:p.Asp1457Asn
  • NP_001394859.1:p.Asp1457Asn
  • NP_001394860.1:p.Asp1457Asn
  • NP_001394861.1:p.Asp1457Asn
  • NP_001394862.1:p.Asp1457Asn
  • NP_001394863.1:p.Asp1456Asn
  • NP_001394864.1:p.Asp1456Asn
  • NP_001394865.1:p.Asp1456Asn
  • NP_001394866.1:p.Asp1505Asn
  • NP_001394867.1:p.Asp1505Asn
  • NP_001394868.1:p.Asp1504Asn
  • NP_001394869.1:p.Asp1504Asn
  • NP_001394870.1:p.Asp1503Asn
  • NP_001394871.1:p.Asp1499Asn
  • NP_001394872.1:p.Asp1498Asn
  • NP_001394873.1:p.Asp1498Asn
  • NP_001394874.1:p.Asp1498Asn
  • NP_001394875.1:p.Asp1435Asn
  • NP_001394876.1:p.Asp1435Asn
  • NP_001394877.1:p.Asp1435Asn
  • NP_001394878.1:p.Asp1435Asn
  • NP_001394879.1:p.Asp1434Asn
  • NP_001394880.1:p.Asp1434Asn
  • NP_001394881.1:p.Asp1434Asn
  • NP_001394882.1:p.Asp1434Asn
  • NP_001394883.1:p.Asp1434Asn
  • NP_001394884.1:p.Asp1434Asn
  • NP_001394885.1:p.Asp1433Asn
  • NP_001394886.1:p.Asp1433Asn
  • NP_001394887.1:p.Asp1433Asn
  • NP_001394888.1:p.Asp1419Asn
  • NP_001394889.1:p.Asp1418Asn
  • NP_001394891.1:p.Asp1418Asn
  • NP_001394892.1:p.Asp1417Asn
  • NP_001394894.1:p.Asp1377Asn
  • NP_001394895.1:p.Asp1250Asn
  • NP_001394896.1:p.Asp1249Asn
  • NP_001394897.1:p.Asp678Asn
  • NP_001394898.1:p.Asp677Asn
  • NP_001394899.1:p.Asp465Asn
  • NP_001394900.1:p.Asp465Asn
  • NP_001394901.1:p.Asp464Asn
  • NP_001394902.1:p.Asp443Asn
  • NP_001394903.1:p.Asp443Asn
  • NP_001394904.1:p.Asp443Asn
  • NP_001394905.1:p.Asp443Asn
  • NP_001394906.1:p.Asp443Asn
  • NP_001394907.1:p.Asp443Asn
  • NP_001394908.1:p.Asp442Asn
  • NP_001394909.1:p.Asp442Asn
  • NP_001394910.1:p.Asp442Asn
  • NP_001394911.1:p.Asp442Asn
  • NP_001394912.1:p.Asp442Asn
  • NP_001394913.1:p.Asp442Asn
  • NP_001394914.1:p.Asp442Asn
  • NP_001394915.1:p.Asp442Asn
  • NP_001394919.1:p.Asp442Asn
  • NP_001394920.1:p.Asp442Asn
  • NP_001394921.1:p.Asp442Asn
  • NP_001394922.1:p.Asp442Asn
  • NP_001395321.1:p.Asp441Asn
  • NP_001395325.1:p.Asp441Asn
  • NP_001395326.1:p.Asp441Asn
  • NP_001395327.1:p.Asp441Asn
  • NP_001395328.1:p.Asp441Asn
  • NP_001395329.1:p.Asp441Asn
  • NP_001395330.1:p.Asp441Asn
  • NP_001395331.1:p.Asp441Asn
  • NP_001395332.1:p.Asp441Asn
  • NP_001395333.1:p.Asp441Asn
  • NP_001395335.1:p.Asp440Asn
  • NP_001395336.1:p.Asp440Asn
  • NP_001395337.1:p.Asp440Asn
  • NP_001395338.1:p.Asp439Asn
  • NP_001395339.1:p.Asp418Asn
  • NP_001395340.1:p.Asp417Asn
  • NP_001395341.1:p.Asp416Asn
  • NP_001395342.1:p.Asp416Asn
  • NP_001395343.1:p.Asp416Asn
  • NP_001395344.1:p.Asp416Asn
  • NP_001395345.1:p.Asp416Asn
  • NP_001395347.1:p.Asp404Asn
  • NP_001395348.1:p.Asp404Asn
  • NP_001395349.1:p.Asp404Asn
  • NP_001395350.1:p.Asp403Asn
  • NP_001395351.1:p.Asp403Asn
  • NP_001395352.1:p.Asp403Asn
  • NP_001395353.1:p.Asp403Asn
  • NP_001395354.1:p.Asp402Asn
  • NP_001395355.1:p.Asp402Asn
  • NP_001395356.1:p.Asp402Asn
  • NP_001395357.1:p.Asp402Asn
  • NP_001395358.1:p.Asp402Asn
  • NP_001395359.1:p.Asp402Asn
  • NP_001395360.1:p.Asp402Asn
  • NP_001395361.1:p.Asp401Asn
  • NP_001395362.1:p.Asp401Asn
  • NP_001395363.1:p.Asp401Asn
  • NP_001395364.1:p.Asp401Asn
  • NP_001395365.1:p.Asp401Asn
  • NP_001395366.1:p.Asp401Asn
  • NP_001395367.1:p.Asp401Asn
  • NP_001395368.1:p.Asp401Asn
  • NP_001395369.1:p.Asp401Asn
  • NP_001395370.1:p.Asp401Asn
  • NP_001395371.1:p.Asp401Asn
  • NP_001395372.1:p.Asp401Asn
  • NP_001395373.1:p.Asp401Asn
  • NP_001395374.1:p.Asp400Asn
  • NP_001395375.1:p.Asp400Asn
  • NP_001395376.1:p.Asp400Asn
  • NP_001395377.1:p.Asp400Asn
  • NP_001395379.1:p.Asp400Asn
  • NP_001395380.1:p.Asp398Asn
  • NP_001395381.1:p.Asp396Asn
  • NP_001395382.1:p.Asp396Asn
  • NP_001395383.1:p.Asp396Asn
  • NP_001395384.1:p.Asp396Asn
  • NP_001395385.1:p.Asp396Asn
  • NP_001395386.1:p.Asp396Asn
  • NP_001395387.1:p.Asp395Asn
  • NP_001395388.1:p.Asp395Asn
  • NP_001395389.1:p.Asp395Asn
  • NP_001395390.1:p.Asp395Asn
  • NP_001395391.1:p.Asp395Asn
  • NP_001395392.1:p.Asp395Asn
  • NP_001395393.1:p.Asp395Asn
  • NP_001395394.1:p.Asp395Asn
  • NP_001395395.1:p.Asp395Asn
  • NP_001395396.1:p.Asp395Asn
  • NP_001395397.1:p.Asp394Asn
  • NP_001395398.1:p.Asp394Asn
  • NP_001395399.1:p.Asp394Asn
  • NP_001395401.1:p.Asp442Asn
  • NP_001395402.1:p.Asp441Asn
  • NP_001395403.1:p.Asp376Asn
  • NP_001395404.1:p.Asp375Asn
  • NP_001395405.1:p.Asp375Asn
  • NP_001395407.1:p.Asp373Asn
  • NP_001395408.1:p.Asp373Asn
  • NP_001395409.1:p.Asp373Asn
  • NP_001395410.1:p.Asp372Asn
  • NP_001395411.1:p.Asp372Asn
  • NP_001395412.1:p.Asp372Asn
  • NP_001395413.1:p.Asp372Asn
  • NP_001395414.1:p.Asp372Asn
  • NP_001395418.1:p.Asp372Asn
  • NP_001395419.1:p.Asp372Asn
  • NP_001395420.1:p.Asp372Asn
  • NP_001395421.1:p.Asp371Asn
  • NP_001395422.1:p.Asp371Asn
  • NP_001395423.1:p.Asp363Asn
  • NP_001395424.1:p.Asp361Asn
  • NP_001395425.1:p.Asp355Asn
  • NP_001395426.1:p.Asp355Asn
  • NP_001395427.1:p.Asp355Asn
  • NP_001395428.1:p.Asp355Asn
  • NP_001395429.1:p.Asp355Asn
  • NP_001395430.1:p.Asp355Asn
  • NP_001395431.1:p.Asp354Asn
  • NP_001395432.1:p.Asp354Asn
  • NP_001395433.1:p.Asp354Asn
  • NP_001395434.1:p.Asp353Asn
  • NP_001395435.1:p.Asp334Asn
  • NP_001395436.1:p.Asp333Asn
  • NP_001395437.1:p.Asp330Asn
  • NP_001395438.1:p.Asp329Asn
  • NP_001395439.1:p.Asp316Asn
  • NP_001395440.1:p.Asp315Asn
  • NP_001395441.1:p.Asp275Asn
  • NP_009225.1:p.Asp1546Asn
  • NP_009225.1:p.Asp1546Asn
  • NP_009228.2:p.Asp1499Asn
  • NP_009229.2:p.Asp442Asn
  • NP_009229.2:p.Asp442Asn
  • NP_009230.2:p.Asp442Asn
  • NP_009231.2:p.Asp1567Asn
  • NP_009235.2:p.Asp442Asn
  • LRG_292t1:c.4636G>A
  • LRG_292:g.143614G>A
  • LRG_292p1:p.Asp1546Asn
  • NC_000017.10:g.41226387C>T
  • NM_007294.3:c.4636G>A
  • NM_007294.4:c.4636G>A
  • NM_007298.3:c.1324G>A
  • NM_007299.3:c.1324G>A
  • NM_007300.3:c.4699G>A
  • NR_027676.2:n.4813G>A
  • U14680.1:n.4755G>A
  • p.D1546N
Protein change:
D1249N
Links:
BRCA1-HCI: BRCA1_00022; dbSNP: rs28897691
NCBI 1000 Genomes Browser:
rs28897691
Molecular consequence:
  • NM_001407571.1:c.4423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407581.1:c.4702G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.4702G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.4699G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.4699G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.4699G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.4696G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.4696G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.4636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.4636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.4636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.4636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.4636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.4636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.4636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.4636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.4627G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.4627G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.4624G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.4621G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.4579G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.4576G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.4636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.4558G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.4558G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.4558G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.4555G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.4555G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.4555G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.4552G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.4552G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.4552G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.4552G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.4552G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.4513G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.4513G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.4513G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.4513G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.4513G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.4513G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.4510G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.4510G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.4510G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.4510G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.4510G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.4510G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.4510G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.4510G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.4510G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.4510G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.4510G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.4507G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.4507G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.4507G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.4636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.4507G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.4507G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.4507G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.4507G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.4507G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.4504G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.4504G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407692.1:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407694.1:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407695.1:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407696.1:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407697.1:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407698.1:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407724.1:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407725.1:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407726.1:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407727.1:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407728.1:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407729.1:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407730.1:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407731.1:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407732.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407733.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407734.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407735.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407736.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407737.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407738.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407739.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407740.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407741.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407742.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407743.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407744.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407745.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407746.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407747.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407748.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407749.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407750.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407751.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407752.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407838.1:c.4489G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407839.1:c.4489G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407841.1:c.4489G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407842.1:c.4489G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407843.1:c.4489G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407844.1:c.4489G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407845.1:c.4489G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407846.1:c.4489G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407847.1:c.4489G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407848.1:c.4489G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407849.1:c.4489G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407850.1:c.4489G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407851.1:c.4489G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407852.1:c.4489G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407853.1:c.4489G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.4636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407858.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407859.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.4633G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407861.1:c.4630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.4435G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.4510G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.4429G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.4429G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407879.1:c.4426G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407881.1:c.4426G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407882.1:c.4426G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407884.1:c.4426G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407885.1:c.4426G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407886.1:c.4426G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407887.1:c.4426G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407889.1:c.4426G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407894.1:c.4423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407895.1:c.4423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407896.1:c.4423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407897.1:c.4423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407898.1:c.4423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407899.1:c.4423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407900.1:c.4423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407902.1:c.4423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407904.1:c.4423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407906.1:c.4423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407907.1:c.4423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407908.1:c.4423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407909.1:c.4423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407910.1:c.4423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407915.1:c.4420G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407916.1:c.4420G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407917.1:c.4420G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407918.1:c.4420G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.4513G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407920.1:c.4372G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407921.1:c.4372G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407922.1:c.4372G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407923.1:c.4372G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407924.1:c.4372G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407925.1:c.4372G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407926.1:c.4372G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407927.1:c.4369G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407928.1:c.4369G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407929.1:c.4369G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407930.1:c.4369G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407931.1:c.4369G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407932.1:c.4369G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407933.1:c.4369G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407934.1:c.4366G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407935.1:c.4366G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407936.1:c.4366G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.4513G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.4513G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407939.1:c.4510G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.4510G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407941.1:c.4507G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407942.1:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407943.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407944.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407945.1:c.4492G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407946.1:c.4303G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407947.1:c.4303G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407948.1:c.4303G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407949.1:c.4303G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407950.1:c.4300G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407951.1:c.4300G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407952.1:c.4300G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407953.1:c.4300G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407954.1:c.4300G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407955.1:c.4300G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407956.1:c.4297G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407957.1:c.4297G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407958.1:c.4297G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407959.1:c.4255G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407960.1:c.4252G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407962.1:c.4252G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407963.1:c.4249G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407965.1:c.4129G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407966.1:c.3748G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407967.1:c.3745G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407968.1:c.2032G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407969.1:c.2029G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407970.1:c.1393G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407971.1:c.1393G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407972.1:c.1390G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407973.1:c.1327G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407974.1:c.1327G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407975.1:c.1327G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407976.1:c.1327G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407977.1:c.1327G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407978.1:c.1327G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407979.1:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407980.1:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407981.1:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407982.1:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407983.1:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407984.1:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407985.1:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407986.1:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407990.1:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407991.1:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407992.1:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407993.1:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408392.1:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408396.1:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408397.1:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408398.1:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408399.1:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408400.1:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408401.1:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408402.1:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408403.1:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408404.1:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408406.1:c.1318G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408407.1:c.1318G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408408.1:c.1318G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408409.1:c.1315G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408410.1:c.1252G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408411.1:c.1249G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408412.1:c.1246G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408413.1:c.1246G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408414.1:c.1246G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408415.1:c.1246G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408416.1:c.1246G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408418.1:c.1210G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408419.1:c.1210G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408420.1:c.1210G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408421.1:c.1207G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408422.1:c.1207G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408423.1:c.1207G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408424.1:c.1207G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408425.1:c.1204G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408426.1:c.1204G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408427.1:c.1204G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408428.1:c.1204G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408429.1:c.1204G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408430.1:c.1204G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408431.1:c.1204G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408432.1:c.1201G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408433.1:c.1201G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408434.1:c.1201G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408435.1:c.1201G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408436.1:c.1201G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408437.1:c.1201G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408438.1:c.1201G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408439.1:c.1201G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408440.1:c.1201G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408441.1:c.1201G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408442.1:c.1201G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408443.1:c.1201G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408444.1:c.1201G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408445.1:c.1198G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408446.1:c.1198G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408447.1:c.1198G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408448.1:c.1198G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408450.1:c.1198G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408451.1:c.1192G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408452.1:c.1186G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408453.1:c.1186G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408454.1:c.1186G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408455.1:c.1186G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408456.1:c.1186G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408457.1:c.1186G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408458.1:c.1183G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408459.1:c.1183G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408460.1:c.1183G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408461.1:c.1183G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408462.1:c.1183G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408463.1:c.1183G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408464.1:c.1183G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408465.1:c.1183G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408466.1:c.1183G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408467.1:c.1183G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408468.1:c.1180G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408469.1:c.1180G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408470.1:c.1180G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408472.1:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408473.1:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408474.1:c.1126G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408475.1:c.1123G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408476.1:c.1123G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408478.1:c.1117G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408479.1:c.1117G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408480.1:c.1117G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408481.1:c.1114G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408482.1:c.1114G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408483.1:c.1114G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408484.1:c.1114G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408485.1:c.1114G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408489.1:c.1114G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408490.1:c.1114G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408491.1:c.1114G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408492.1:c.1111G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408493.1:c.1111G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408494.1:c.1087G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408495.1:c.1081G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408496.1:c.1063G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408497.1:c.1063G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408498.1:c.1063G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408499.1:c.1063G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408500.1:c.1063G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408501.1:c.1063G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408502.1:c.1060G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408503.1:c.1060G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408504.1:c.1060G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408505.1:c.1057G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408506.1:c.1000G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408507.1:c.997G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408508.1:c.988G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408509.1:c.985G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408510.1:c.946G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408511.1:c.943G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408512.1:c.823G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.4636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007297.4:c.4495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007298.4:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007299.4:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.4699G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007304.2:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_027676.2:n.4813G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000167307GeneDx
criteria provided, single submitter

(GeneDx Variant Classification (06012015))
Benign
(Dec 13, 2013)
germlineclinical testing

Citation Link,

SCV000806956PreventionGenetics, part of Exact Sciences
criteria provided, single submitter

(ACMG Guidelines, 2015)
Benign
(Mar 31, 2017)
germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

SCV001906156Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute - VKGL Data-share Consensus

See additional submitters

no assertion criteria provided
Benigngermlineclinical testing

SCV001959251Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ - VKGL Data-share Consensus

See additional submitters

no assertion criteria provided
Benigngermlineclinical testing

SCV002065803Genetic Services Laboratory, University of Chicago
criteria provided, single submitter

(ACMG Guidelines, 2015)
Likely benign
(Aug 24, 2021)
germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

SCV002550971Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital
criteria provided, single submitter

(ACMG Guidelines, 2015)
Benign
(Aug 15, 2023)
germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenonot providednot providednot providednot providednot providedclinical testing
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From GeneDx, SCV000167307.11

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

From PreventionGenetics, part of Exact Sciences, SCV000806956.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

From Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute - VKGL Data-share Consensus, SCV001906156.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

From Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ - VKGL Data-share Consensus, SCV001959251.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

From Genetic Services Laboratory, University of Chicago, SCV002065803.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlinenonot providednot providednot providednot providednot providednot providednot provided

From Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital, SCV002550971.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 13, 2024