U.S. flag

An official website of the United States government

NM_007294.4(BRCA1):c.4641G>T (p.Leu1547Phe) AND Hereditary breast ovarian cancer syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 7, 2016
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
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:
RCV000206692.7

Allele description [Variation Report for NM_007294.4(BRCA1):c.4641G>T (p.Leu1547Phe)]

NM_007294.4(BRCA1):c.4641G>T (p.Leu1547Phe)

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.4641G>T (p.Leu1547Phe)
HGVS:
  • NC_000017.11:g.43074365C>A
  • NG_005905.2:g.143619G>T
  • NM_001407571.1:c.4428G>T
  • NM_001407581.1:c.4707G>T
  • NM_001407582.1:c.4707G>T
  • NM_001407583.1:c.4704G>T
  • NM_001407585.1:c.4704G>T
  • NM_001407587.1:c.4704G>T
  • NM_001407590.1:c.4701G>T
  • NM_001407591.1:c.4701G>T
  • NM_001407593.1:c.4641G>T
  • NM_001407594.1:c.4641G>T
  • NM_001407596.1:c.4641G>T
  • NM_001407597.1:c.4641G>T
  • NM_001407598.1:c.4641G>T
  • NM_001407602.1:c.4641G>T
  • NM_001407603.1:c.4641G>T
  • NM_001407605.1:c.4641G>T
  • NM_001407610.1:c.4638G>T
  • NM_001407611.1:c.4638G>T
  • NM_001407612.1:c.4638G>T
  • NM_001407613.1:c.4638G>T
  • NM_001407614.1:c.4638G>T
  • NM_001407615.1:c.4638G>T
  • NM_001407616.1:c.4638G>T
  • NM_001407617.1:c.4638G>T
  • NM_001407618.1:c.4638G>T
  • NM_001407619.1:c.4638G>T
  • NM_001407620.1:c.4638G>T
  • NM_001407621.1:c.4638G>T
  • NM_001407622.1:c.4638G>T
  • NM_001407623.1:c.4638G>T
  • NM_001407624.1:c.4638G>T
  • NM_001407625.1:c.4638G>T
  • NM_001407626.1:c.4638G>T
  • NM_001407627.1:c.4635G>T
  • NM_001407628.1:c.4635G>T
  • NM_001407629.1:c.4635G>T
  • NM_001407630.1:c.4635G>T
  • NM_001407631.1:c.4635G>T
  • NM_001407632.1:c.4635G>T
  • NM_001407633.1:c.4635G>T
  • NM_001407634.1:c.4635G>T
  • NM_001407635.1:c.4635G>T
  • NM_001407636.1:c.4635G>T
  • NM_001407637.1:c.4635G>T
  • NM_001407638.1:c.4635G>T
  • NM_001407639.1:c.4635G>T
  • NM_001407640.1:c.4635G>T
  • NM_001407641.1:c.4635G>T
  • NM_001407642.1:c.4635G>T
  • NM_001407644.1:c.4632G>T
  • NM_001407645.1:c.4632G>T
  • NM_001407646.1:c.4629G>T
  • NM_001407647.1:c.4626G>T
  • NM_001407648.1:c.4584G>T
  • NM_001407649.1:c.4581G>T
  • NM_001407652.1:c.4641G>T
  • NM_001407653.1:c.4563G>T
  • NM_001407654.1:c.4563G>T
  • NM_001407655.1:c.4563G>T
  • NM_001407656.1:c.4560G>T
  • NM_001407657.1:c.4560G>T
  • NM_001407658.1:c.4560G>T
  • NM_001407659.1:c.4557G>T
  • NM_001407660.1:c.4557G>T
  • NM_001407661.1:c.4557G>T
  • NM_001407662.1:c.4557G>T
  • NM_001407663.1:c.4557G>T
  • NM_001407664.1:c.4518G>T
  • NM_001407665.1:c.4518G>T
  • NM_001407666.1:c.4518G>T
  • NM_001407667.1:c.4518G>T
  • NM_001407668.1:c.4518G>T
  • NM_001407669.1:c.4518G>T
  • NM_001407670.1:c.4515G>T
  • NM_001407671.1:c.4515G>T
  • NM_001407672.1:c.4515G>T
  • NM_001407673.1:c.4515G>T
  • NM_001407674.1:c.4515G>T
  • NM_001407675.1:c.4515G>T
  • NM_001407676.1:c.4515G>T
  • NM_001407677.1:c.4515G>T
  • NM_001407678.1:c.4515G>T
  • NM_001407679.1:c.4515G>T
  • NM_001407680.1:c.4515G>T
  • NM_001407681.1:c.4512G>T
  • NM_001407682.1:c.4512G>T
  • NM_001407683.1:c.4512G>T
  • NM_001407684.1:c.4641G>T
  • NM_001407685.1:c.4512G>T
  • NM_001407686.1:c.4512G>T
  • NM_001407687.1:c.4512G>T
  • NM_001407688.1:c.4512G>T
  • NM_001407689.1:c.4512G>T
  • NM_001407690.1:c.4509G>T
  • NM_001407691.1:c.4509G>T
  • NM_001407692.1:c.4500G>T
  • NM_001407694.1:c.4500G>T
  • NM_001407695.1:c.4500G>T
  • NM_001407696.1:c.4500G>T
  • NM_001407697.1:c.4500G>T
  • NM_001407698.1:c.4500G>T
  • NM_001407724.1:c.4500G>T
  • NM_001407725.1:c.4500G>T
  • NM_001407726.1:c.4500G>T
  • NM_001407727.1:c.4500G>T
  • NM_001407728.1:c.4500G>T
  • NM_001407729.1:c.4500G>T
  • NM_001407730.1:c.4500G>T
  • NM_001407731.1:c.4500G>T
  • NM_001407732.1:c.4497G>T
  • NM_001407733.1:c.4497G>T
  • NM_001407734.1:c.4497G>T
  • NM_001407735.1:c.4497G>T
  • NM_001407736.1:c.4497G>T
  • NM_001407737.1:c.4497G>T
  • NM_001407738.1:c.4497G>T
  • NM_001407739.1:c.4497G>T
  • NM_001407740.1:c.4497G>T
  • NM_001407741.1:c.4497G>T
  • NM_001407742.1:c.4497G>T
  • NM_001407743.1:c.4497G>T
  • NM_001407744.1:c.4497G>T
  • NM_001407745.1:c.4497G>T
  • NM_001407746.1:c.4497G>T
  • NM_001407747.1:c.4497G>T
  • NM_001407748.1:c.4497G>T
  • NM_001407749.1:c.4497G>T
  • NM_001407750.1:c.4497G>T
  • NM_001407751.1:c.4497G>T
  • NM_001407752.1:c.4497G>T
  • NM_001407838.1:c.4494G>T
  • NM_001407839.1:c.4494G>T
  • NM_001407841.1:c.4494G>T
  • NM_001407842.1:c.4494G>T
  • NM_001407843.1:c.4494G>T
  • NM_001407844.1:c.4494G>T
  • NM_001407845.1:c.4494G>T
  • NM_001407846.1:c.4494G>T
  • NM_001407847.1:c.4494G>T
  • NM_001407848.1:c.4494G>T
  • NM_001407849.1:c.4494G>T
  • NM_001407850.1:c.4494G>T
  • NM_001407851.1:c.4494G>T
  • NM_001407852.1:c.4494G>T
  • NM_001407853.1:c.4494G>T
  • NM_001407854.1:c.4641G>T
  • NM_001407858.1:c.4638G>T
  • NM_001407859.1:c.4638G>T
  • NM_001407860.1:c.4638G>T
  • NM_001407861.1:c.4635G>T
  • NM_001407862.1:c.4440G>T
  • NM_001407863.1:c.4515G>T
  • NM_001407874.1:c.4434G>T
  • NM_001407875.1:c.4434G>T
  • NM_001407879.1:c.4431G>T
  • NM_001407881.1:c.4431G>T
  • NM_001407882.1:c.4431G>T
  • NM_001407884.1:c.4431G>T
  • NM_001407885.1:c.4431G>T
  • NM_001407886.1:c.4431G>T
  • NM_001407887.1:c.4431G>T
  • NM_001407889.1:c.4431G>T
  • NM_001407894.1:c.4428G>T
  • NM_001407895.1:c.4428G>T
  • NM_001407896.1:c.4428G>T
  • NM_001407897.1:c.4428G>T
  • NM_001407898.1:c.4428G>T
  • NM_001407899.1:c.4428G>T
  • NM_001407900.1:c.4428G>T
  • NM_001407902.1:c.4428G>T
  • NM_001407904.1:c.4428G>T
  • NM_001407906.1:c.4428G>T
  • NM_001407907.1:c.4428G>T
  • NM_001407908.1:c.4428G>T
  • NM_001407909.1:c.4428G>T
  • NM_001407910.1:c.4428G>T
  • NM_001407915.1:c.4425G>T
  • NM_001407916.1:c.4425G>T
  • NM_001407917.1:c.4425G>T
  • NM_001407918.1:c.4425G>T
  • NM_001407919.1:c.4518G>T
  • NM_001407920.1:c.4377G>T
  • NM_001407921.1:c.4377G>T
  • NM_001407922.1:c.4377G>T
  • NM_001407923.1:c.4377G>T
  • NM_001407924.1:c.4377G>T
  • NM_001407925.1:c.4377G>T
  • NM_001407926.1:c.4377G>T
  • NM_001407927.1:c.4374G>T
  • NM_001407928.1:c.4374G>T
  • NM_001407929.1:c.4374G>T
  • NM_001407930.1:c.4374G>T
  • NM_001407931.1:c.4374G>T
  • NM_001407932.1:c.4374G>T
  • NM_001407933.1:c.4374G>T
  • NM_001407934.1:c.4371G>T
  • NM_001407935.1:c.4371G>T
  • NM_001407936.1:c.4371G>T
  • NM_001407937.1:c.4518G>T
  • NM_001407938.1:c.4518G>T
  • NM_001407939.1:c.4515G>T
  • NM_001407940.1:c.4515G>T
  • NM_001407941.1:c.4512G>T
  • NM_001407942.1:c.4500G>T
  • NM_001407943.1:c.4497G>T
  • NM_001407944.1:c.4497G>T
  • NM_001407945.1:c.4497G>T
  • NM_001407946.1:c.4308G>T
  • NM_001407947.1:c.4308G>T
  • NM_001407948.1:c.4308G>T
  • NM_001407949.1:c.4308G>T
  • NM_001407950.1:c.4305G>T
  • NM_001407951.1:c.4305G>T
  • NM_001407952.1:c.4305G>T
  • NM_001407953.1:c.4305G>T
  • NM_001407954.1:c.4305G>T
  • NM_001407955.1:c.4305G>T
  • NM_001407956.1:c.4302G>T
  • NM_001407957.1:c.4302G>T
  • NM_001407958.1:c.4302G>T
  • NM_001407959.1:c.4260G>T
  • NM_001407960.1:c.4257G>T
  • NM_001407962.1:c.4257G>T
  • NM_001407963.1:c.4254G>T
  • NM_001407965.1:c.4134G>T
  • NM_001407966.1:c.3753G>T
  • NM_001407967.1:c.3750G>T
  • NM_001407968.1:c.2037G>T
  • NM_001407969.1:c.2034G>T
  • NM_001407970.1:c.1398G>T
  • NM_001407971.1:c.1398G>T
  • NM_001407972.1:c.1395G>T
  • NM_001407973.1:c.1332G>T
  • NM_001407974.1:c.1332G>T
  • NM_001407975.1:c.1332G>T
  • NM_001407976.1:c.1332G>T
  • NM_001407977.1:c.1332G>T
  • NM_001407978.1:c.1332G>T
  • NM_001407979.1:c.1329G>T
  • NM_001407980.1:c.1329G>T
  • NM_001407981.1:c.1329G>T
  • NM_001407982.1:c.1329G>T
  • NM_001407983.1:c.1329G>T
  • NM_001407984.1:c.1329G>T
  • NM_001407985.1:c.1329G>T
  • NM_001407986.1:c.1329G>T
  • NM_001407990.1:c.1329G>T
  • NM_001407991.1:c.1329G>T
  • NM_001407992.1:c.1329G>T
  • NM_001407993.1:c.1329G>T
  • NM_001408392.1:c.1326G>T
  • NM_001408396.1:c.1326G>T
  • NM_001408397.1:c.1326G>T
  • NM_001408398.1:c.1326G>T
  • NM_001408399.1:c.1326G>T
  • NM_001408400.1:c.1326G>T
  • NM_001408401.1:c.1326G>T
  • NM_001408402.1:c.1326G>T
  • NM_001408403.1:c.1326G>T
  • NM_001408404.1:c.1326G>T
  • NM_001408406.1:c.1323G>T
  • NM_001408407.1:c.1323G>T
  • NM_001408408.1:c.1323G>T
  • NM_001408409.1:c.1320G>T
  • NM_001408410.1:c.1257G>T
  • NM_001408411.1:c.1254G>T
  • NM_001408412.1:c.1251G>T
  • NM_001408413.1:c.1251G>T
  • NM_001408414.1:c.1251G>T
  • NM_001408415.1:c.1251G>T
  • NM_001408416.1:c.1251G>T
  • NM_001408418.1:c.1215G>T
  • NM_001408419.1:c.1215G>T
  • NM_001408420.1:c.1215G>T
  • NM_001408421.1:c.1212G>T
  • NM_001408422.1:c.1212G>T
  • NM_001408423.1:c.1212G>T
  • NM_001408424.1:c.1212G>T
  • NM_001408425.1:c.1209G>T
  • NM_001408426.1:c.1209G>T
  • NM_001408427.1:c.1209G>T
  • NM_001408428.1:c.1209G>T
  • NM_001408429.1:c.1209G>T
  • NM_001408430.1:c.1209G>T
  • NM_001408431.1:c.1209G>T
  • NM_001408432.1:c.1206G>T
  • NM_001408433.1:c.1206G>T
  • NM_001408434.1:c.1206G>T
  • NM_001408435.1:c.1206G>T
  • NM_001408436.1:c.1206G>T
  • NM_001408437.1:c.1206G>T
  • NM_001408438.1:c.1206G>T
  • NM_001408439.1:c.1206G>T
  • NM_001408440.1:c.1206G>T
  • NM_001408441.1:c.1206G>T
  • NM_001408442.1:c.1206G>T
  • NM_001408443.1:c.1206G>T
  • NM_001408444.1:c.1206G>T
  • NM_001408445.1:c.1203G>T
  • NM_001408446.1:c.1203G>T
  • NM_001408447.1:c.1203G>T
  • NM_001408448.1:c.1203G>T
  • NM_001408450.1:c.1203G>T
  • NM_001408451.1:c.1197G>T
  • NM_001408452.1:c.1191G>T
  • NM_001408453.1:c.1191G>T
  • NM_001408454.1:c.1191G>T
  • NM_001408455.1:c.1191G>T
  • NM_001408456.1:c.1191G>T
  • NM_001408457.1:c.1191G>T
  • NM_001408458.1:c.1188G>T
  • NM_001408459.1:c.1188G>T
  • NM_001408460.1:c.1188G>T
  • NM_001408461.1:c.1188G>T
  • NM_001408462.1:c.1188G>T
  • NM_001408463.1:c.1188G>T
  • NM_001408464.1:c.1188G>T
  • NM_001408465.1:c.1188G>T
  • NM_001408466.1:c.1188G>T
  • NM_001408467.1:c.1188G>T
  • NM_001408468.1:c.1185G>T
  • NM_001408469.1:c.1185G>T
  • NM_001408470.1:c.1185G>T
  • NM_001408472.1:c.1329G>T
  • NM_001408473.1:c.1326G>T
  • NM_001408474.1:c.1131G>T
  • NM_001408475.1:c.1128G>T
  • NM_001408476.1:c.1128G>T
  • NM_001408478.1:c.1122G>T
  • NM_001408479.1:c.1122G>T
  • NM_001408480.1:c.1122G>T
  • NM_001408481.1:c.1119G>T
  • NM_001408482.1:c.1119G>T
  • NM_001408483.1:c.1119G>T
  • NM_001408484.1:c.1119G>T
  • NM_001408485.1:c.1119G>T
  • NM_001408489.1:c.1119G>T
  • NM_001408490.1:c.1119G>T
  • NM_001408491.1:c.1119G>T
  • NM_001408492.1:c.1116G>T
  • NM_001408493.1:c.1116G>T
  • NM_001408494.1:c.1092G>T
  • NM_001408495.1:c.1086G>T
  • NM_001408496.1:c.1068G>T
  • NM_001408497.1:c.1068G>T
  • NM_001408498.1:c.1068G>T
  • NM_001408499.1:c.1068G>T
  • NM_001408500.1:c.1068G>T
  • NM_001408501.1:c.1068G>T
  • NM_001408502.1:c.1065G>T
  • NM_001408503.1:c.1065G>T
  • NM_001408504.1:c.1065G>T
  • NM_001408505.1:c.1062G>T
  • NM_001408506.1:c.1005G>T
  • NM_001408507.1:c.1002G>T
  • NM_001408508.1:c.993G>T
  • NM_001408509.1:c.990G>T
  • NM_001408510.1:c.951G>T
  • NM_001408511.1:c.948G>T
  • NM_001408512.1:c.828G>T
  • NM_007294.4:c.4641G>TMANE SELECT
  • NM_007297.4:c.4500G>T
  • NM_007298.4:c.1329G>T
  • NM_007299.4:c.1329G>T
  • NM_007300.4:c.4704G>T
  • NM_007304.2:c.1329G>T
  • NP_001394500.1:p.Leu1476Phe
  • NP_001394510.1:p.Leu1569Phe
  • NP_001394511.1:p.Leu1569Phe
  • NP_001394512.1:p.Leu1568Phe
  • NP_001394514.1:p.Leu1568Phe
  • NP_001394516.1:p.Leu1568Phe
  • NP_001394519.1:p.Leu1567Phe
  • NP_001394520.1:p.Leu1567Phe
  • NP_001394522.1:p.Leu1547Phe
  • NP_001394523.1:p.Leu1547Phe
  • NP_001394525.1:p.Leu1547Phe
  • NP_001394526.1:p.Leu1547Phe
  • NP_001394527.1:p.Leu1547Phe
  • NP_001394531.1:p.Leu1547Phe
  • NP_001394532.1:p.Leu1547Phe
  • NP_001394534.1:p.Leu1547Phe
  • NP_001394539.1:p.Leu1546Phe
  • NP_001394540.1:p.Leu1546Phe
  • NP_001394541.1:p.Leu1546Phe
  • NP_001394542.1:p.Leu1546Phe
  • NP_001394543.1:p.Leu1546Phe
  • NP_001394544.1:p.Leu1546Phe
  • NP_001394545.1:p.Leu1546Phe
  • NP_001394546.1:p.Leu1546Phe
  • NP_001394547.1:p.Leu1546Phe
  • NP_001394548.1:p.Leu1546Phe
  • NP_001394549.1:p.Leu1546Phe
  • NP_001394550.1:p.Leu1546Phe
  • NP_001394551.1:p.Leu1546Phe
  • NP_001394552.1:p.Leu1546Phe
  • NP_001394553.1:p.Leu1546Phe
  • NP_001394554.1:p.Leu1546Phe
  • NP_001394555.1:p.Leu1546Phe
  • NP_001394556.1:p.Leu1545Phe
  • NP_001394557.1:p.Leu1545Phe
  • NP_001394558.1:p.Leu1545Phe
  • NP_001394559.1:p.Leu1545Phe
  • NP_001394560.1:p.Leu1545Phe
  • NP_001394561.1:p.Leu1545Phe
  • NP_001394562.1:p.Leu1545Phe
  • NP_001394563.1:p.Leu1545Phe
  • NP_001394564.1:p.Leu1545Phe
  • NP_001394565.1:p.Leu1545Phe
  • NP_001394566.1:p.Leu1545Phe
  • NP_001394567.1:p.Leu1545Phe
  • NP_001394568.1:p.Leu1545Phe
  • NP_001394569.1:p.Leu1545Phe
  • NP_001394570.1:p.Leu1545Phe
  • NP_001394571.1:p.Leu1545Phe
  • NP_001394573.1:p.Leu1544Phe
  • NP_001394574.1:p.Leu1544Phe
  • NP_001394575.1:p.Leu1543Phe
  • NP_001394576.1:p.Leu1542Phe
  • NP_001394577.1:p.Leu1528Phe
  • NP_001394578.1:p.Leu1527Phe
  • NP_001394581.1:p.Leu1547Phe
  • NP_001394582.1:p.Leu1521Phe
  • NP_001394583.1:p.Leu1521Phe
  • NP_001394584.1:p.Leu1521Phe
  • NP_001394585.1:p.Leu1520Phe
  • NP_001394586.1:p.Leu1520Phe
  • NP_001394587.1:p.Leu1520Phe
  • NP_001394588.1:p.Leu1519Phe
  • NP_001394589.1:p.Leu1519Phe
  • NP_001394590.1:p.Leu1519Phe
  • NP_001394591.1:p.Leu1519Phe
  • NP_001394592.1:p.Leu1519Phe
  • NP_001394593.1:p.Leu1506Phe
  • NP_001394594.1:p.Leu1506Phe
  • NP_001394595.1:p.Leu1506Phe
  • NP_001394596.1:p.Leu1506Phe
  • NP_001394597.1:p.Leu1506Phe
  • NP_001394598.1:p.Leu1506Phe
  • NP_001394599.1:p.Leu1505Phe
  • NP_001394600.1:p.Leu1505Phe
  • NP_001394601.1:p.Leu1505Phe
  • NP_001394602.1:p.Leu1505Phe
  • NP_001394603.1:p.Leu1505Phe
  • NP_001394604.1:p.Leu1505Phe
  • NP_001394605.1:p.Leu1505Phe
  • NP_001394606.1:p.Leu1505Phe
  • NP_001394607.1:p.Leu1505Phe
  • NP_001394608.1:p.Leu1505Phe
  • NP_001394609.1:p.Leu1505Phe
  • NP_001394610.1:p.Leu1504Phe
  • NP_001394611.1:p.Leu1504Phe
  • NP_001394612.1:p.Leu1504Phe
  • NP_001394613.1:p.Leu1547Phe
  • NP_001394614.1:p.Leu1504Phe
  • NP_001394615.1:p.Leu1504Phe
  • NP_001394616.1:p.Leu1504Phe
  • NP_001394617.1:p.Leu1504Phe
  • NP_001394618.1:p.Leu1504Phe
  • NP_001394619.1:p.Leu1503Phe
  • NP_001394620.1:p.Leu1503Phe
  • NP_001394621.1:p.Leu1500Phe
  • NP_001394623.1:p.Leu1500Phe
  • NP_001394624.1:p.Leu1500Phe
  • NP_001394625.1:p.Leu1500Phe
  • NP_001394626.1:p.Leu1500Phe
  • NP_001394627.1:p.Leu1500Phe
  • NP_001394653.1:p.Leu1500Phe
  • NP_001394654.1:p.Leu1500Phe
  • NP_001394655.1:p.Leu1500Phe
  • NP_001394656.1:p.Leu1500Phe
  • NP_001394657.1:p.Leu1500Phe
  • NP_001394658.1:p.Leu1500Phe
  • NP_001394659.1:p.Leu1500Phe
  • NP_001394660.1:p.Leu1500Phe
  • NP_001394661.1:p.Leu1499Phe
  • NP_001394662.1:p.Leu1499Phe
  • NP_001394663.1:p.Leu1499Phe
  • NP_001394664.1:p.Leu1499Phe
  • NP_001394665.1:p.Leu1499Phe
  • NP_001394666.1:p.Leu1499Phe
  • NP_001394667.1:p.Leu1499Phe
  • NP_001394668.1:p.Leu1499Phe
  • NP_001394669.1:p.Leu1499Phe
  • NP_001394670.1:p.Leu1499Phe
  • NP_001394671.1:p.Leu1499Phe
  • NP_001394672.1:p.Leu1499Phe
  • NP_001394673.1:p.Leu1499Phe
  • NP_001394674.1:p.Leu1499Phe
  • NP_001394675.1:p.Leu1499Phe
  • NP_001394676.1:p.Leu1499Phe
  • NP_001394677.1:p.Leu1499Phe
  • NP_001394678.1:p.Leu1499Phe
  • NP_001394679.1:p.Leu1499Phe
  • NP_001394680.1:p.Leu1499Phe
  • NP_001394681.1:p.Leu1499Phe
  • NP_001394767.1:p.Leu1498Phe
  • NP_001394768.1:p.Leu1498Phe
  • NP_001394770.1:p.Leu1498Phe
  • NP_001394771.1:p.Leu1498Phe
  • NP_001394772.1:p.Leu1498Phe
  • NP_001394773.1:p.Leu1498Phe
  • NP_001394774.1:p.Leu1498Phe
  • NP_001394775.1:p.Leu1498Phe
  • NP_001394776.1:p.Leu1498Phe
  • NP_001394777.1:p.Leu1498Phe
  • NP_001394778.1:p.Leu1498Phe
  • NP_001394779.1:p.Leu1498Phe
  • NP_001394780.1:p.Leu1498Phe
  • NP_001394781.1:p.Leu1498Phe
  • NP_001394782.1:p.Leu1498Phe
  • NP_001394783.1:p.Leu1547Phe
  • NP_001394787.1:p.Leu1546Phe
  • NP_001394788.1:p.Leu1546Phe
  • NP_001394789.1:p.Leu1546Phe
  • NP_001394790.1:p.Leu1545Phe
  • NP_001394791.1:p.Leu1480Phe
  • NP_001394792.1:p.Leu1505Phe
  • NP_001394803.1:p.Leu1478Phe
  • NP_001394804.1:p.Leu1478Phe
  • NP_001394808.1:p.Leu1477Phe
  • NP_001394810.1:p.Leu1477Phe
  • NP_001394811.1:p.Leu1477Phe
  • NP_001394813.1:p.Leu1477Phe
  • NP_001394814.1:p.Leu1477Phe
  • NP_001394815.1:p.Leu1477Phe
  • NP_001394816.1:p.Leu1477Phe
  • NP_001394818.1:p.Leu1477Phe
  • NP_001394823.1:p.Leu1476Phe
  • NP_001394824.1:p.Leu1476Phe
  • NP_001394825.1:p.Leu1476Phe
  • NP_001394826.1:p.Leu1476Phe
  • NP_001394827.1:p.Leu1476Phe
  • NP_001394828.1:p.Leu1476Phe
  • NP_001394829.1:p.Leu1476Phe
  • NP_001394831.1:p.Leu1476Phe
  • NP_001394833.1:p.Leu1476Phe
  • NP_001394835.1:p.Leu1476Phe
  • NP_001394836.1:p.Leu1476Phe
  • NP_001394837.1:p.Leu1476Phe
  • NP_001394838.1:p.Leu1476Phe
  • NP_001394839.1:p.Leu1476Phe
  • NP_001394844.1:p.Leu1475Phe
  • NP_001394845.1:p.Leu1475Phe
  • NP_001394846.1:p.Leu1475Phe
  • NP_001394847.1:p.Leu1475Phe
  • NP_001394848.1:p.Leu1506Phe
  • NP_001394849.1:p.Leu1459Phe
  • NP_001394850.1:p.Leu1459Phe
  • NP_001394851.1:p.Leu1459Phe
  • NP_001394852.1:p.Leu1459Phe
  • NP_001394853.1:p.Leu1459Phe
  • NP_001394854.1:p.Leu1459Phe
  • NP_001394855.1:p.Leu1459Phe
  • NP_001394856.1:p.Leu1458Phe
  • NP_001394857.1:p.Leu1458Phe
  • NP_001394858.1:p.Leu1458Phe
  • NP_001394859.1:p.Leu1458Phe
  • NP_001394860.1:p.Leu1458Phe
  • NP_001394861.1:p.Leu1458Phe
  • NP_001394862.1:p.Leu1458Phe
  • NP_001394863.1:p.Leu1457Phe
  • NP_001394864.1:p.Leu1457Phe
  • NP_001394865.1:p.Leu1457Phe
  • NP_001394866.1:p.Leu1506Phe
  • NP_001394867.1:p.Leu1506Phe
  • NP_001394868.1:p.Leu1505Phe
  • NP_001394869.1:p.Leu1505Phe
  • NP_001394870.1:p.Leu1504Phe
  • NP_001394871.1:p.Leu1500Phe
  • NP_001394872.1:p.Leu1499Phe
  • NP_001394873.1:p.Leu1499Phe
  • NP_001394874.1:p.Leu1499Phe
  • NP_001394875.1:p.Leu1436Phe
  • NP_001394876.1:p.Leu1436Phe
  • NP_001394877.1:p.Leu1436Phe
  • NP_001394878.1:p.Leu1436Phe
  • NP_001394879.1:p.Leu1435Phe
  • NP_001394880.1:p.Leu1435Phe
  • NP_001394881.1:p.Leu1435Phe
  • NP_001394882.1:p.Leu1435Phe
  • NP_001394883.1:p.Leu1435Phe
  • NP_001394884.1:p.Leu1435Phe
  • NP_001394885.1:p.Leu1434Phe
  • NP_001394886.1:p.Leu1434Phe
  • NP_001394887.1:p.Leu1434Phe
  • NP_001394888.1:p.Leu1420Phe
  • NP_001394889.1:p.Leu1419Phe
  • NP_001394891.1:p.Leu1419Phe
  • NP_001394892.1:p.Leu1418Phe
  • NP_001394894.1:p.Leu1378Phe
  • NP_001394895.1:p.Leu1251Phe
  • NP_001394896.1:p.Leu1250Phe
  • NP_001394897.1:p.Leu679Phe
  • NP_001394898.1:p.Leu678Phe
  • NP_001394899.1:p.Leu466Phe
  • NP_001394900.1:p.Leu466Phe
  • NP_001394901.1:p.Leu465Phe
  • NP_001394902.1:p.Leu444Phe
  • NP_001394903.1:p.Leu444Phe
  • NP_001394904.1:p.Leu444Phe
  • NP_001394905.1:p.Leu444Phe
  • NP_001394906.1:p.Leu444Phe
  • NP_001394907.1:p.Leu444Phe
  • NP_001394908.1:p.Leu443Phe
  • NP_001394909.1:p.Leu443Phe
  • NP_001394910.1:p.Leu443Phe
  • NP_001394911.1:p.Leu443Phe
  • NP_001394912.1:p.Leu443Phe
  • NP_001394913.1:p.Leu443Phe
  • NP_001394914.1:p.Leu443Phe
  • NP_001394915.1:p.Leu443Phe
  • NP_001394919.1:p.Leu443Phe
  • NP_001394920.1:p.Leu443Phe
  • NP_001394921.1:p.Leu443Phe
  • NP_001394922.1:p.Leu443Phe
  • NP_001395321.1:p.Leu442Phe
  • NP_001395325.1:p.Leu442Phe
  • NP_001395326.1:p.Leu442Phe
  • NP_001395327.1:p.Leu442Phe
  • NP_001395328.1:p.Leu442Phe
  • NP_001395329.1:p.Leu442Phe
  • NP_001395330.1:p.Leu442Phe
  • NP_001395331.1:p.Leu442Phe
  • NP_001395332.1:p.Leu442Phe
  • NP_001395333.1:p.Leu442Phe
  • NP_001395335.1:p.Leu441Phe
  • NP_001395336.1:p.Leu441Phe
  • NP_001395337.1:p.Leu441Phe
  • NP_001395338.1:p.Leu440Phe
  • NP_001395339.1:p.Leu419Phe
  • NP_001395340.1:p.Leu418Phe
  • NP_001395341.1:p.Leu417Phe
  • NP_001395342.1:p.Leu417Phe
  • NP_001395343.1:p.Leu417Phe
  • NP_001395344.1:p.Leu417Phe
  • NP_001395345.1:p.Leu417Phe
  • NP_001395347.1:p.Leu405Phe
  • NP_001395348.1:p.Leu405Phe
  • NP_001395349.1:p.Leu405Phe
  • NP_001395350.1:p.Leu404Phe
  • NP_001395351.1:p.Leu404Phe
  • NP_001395352.1:p.Leu404Phe
  • NP_001395353.1:p.Leu404Phe
  • NP_001395354.1:p.Leu403Phe
  • NP_001395355.1:p.Leu403Phe
  • NP_001395356.1:p.Leu403Phe
  • NP_001395357.1:p.Leu403Phe
  • NP_001395358.1:p.Leu403Phe
  • NP_001395359.1:p.Leu403Phe
  • NP_001395360.1:p.Leu403Phe
  • NP_001395361.1:p.Leu402Phe
  • NP_001395362.1:p.Leu402Phe
  • NP_001395363.1:p.Leu402Phe
  • NP_001395364.1:p.Leu402Phe
  • NP_001395365.1:p.Leu402Phe
  • NP_001395366.1:p.Leu402Phe
  • NP_001395367.1:p.Leu402Phe
  • NP_001395368.1:p.Leu402Phe
  • NP_001395369.1:p.Leu402Phe
  • NP_001395370.1:p.Leu402Phe
  • NP_001395371.1:p.Leu402Phe
  • NP_001395372.1:p.Leu402Phe
  • NP_001395373.1:p.Leu402Phe
  • NP_001395374.1:p.Leu401Phe
  • NP_001395375.1:p.Leu401Phe
  • NP_001395376.1:p.Leu401Phe
  • NP_001395377.1:p.Leu401Phe
  • NP_001395379.1:p.Leu401Phe
  • NP_001395380.1:p.Leu399Phe
  • NP_001395381.1:p.Leu397Phe
  • NP_001395382.1:p.Leu397Phe
  • NP_001395383.1:p.Leu397Phe
  • NP_001395384.1:p.Leu397Phe
  • NP_001395385.1:p.Leu397Phe
  • NP_001395386.1:p.Leu397Phe
  • NP_001395387.1:p.Leu396Phe
  • NP_001395388.1:p.Leu396Phe
  • NP_001395389.1:p.Leu396Phe
  • NP_001395390.1:p.Leu396Phe
  • NP_001395391.1:p.Leu396Phe
  • NP_001395392.1:p.Leu396Phe
  • NP_001395393.1:p.Leu396Phe
  • NP_001395394.1:p.Leu396Phe
  • NP_001395395.1:p.Leu396Phe
  • NP_001395396.1:p.Leu396Phe
  • NP_001395397.1:p.Leu395Phe
  • NP_001395398.1:p.Leu395Phe
  • NP_001395399.1:p.Leu395Phe
  • NP_001395401.1:p.Leu443Phe
  • NP_001395402.1:p.Leu442Phe
  • NP_001395403.1:p.Leu377Phe
  • NP_001395404.1:p.Leu376Phe
  • NP_001395405.1:p.Leu376Phe
  • NP_001395407.1:p.Leu374Phe
  • NP_001395408.1:p.Leu374Phe
  • NP_001395409.1:p.Leu374Phe
  • NP_001395410.1:p.Leu373Phe
  • NP_001395411.1:p.Leu373Phe
  • NP_001395412.1:p.Leu373Phe
  • NP_001395413.1:p.Leu373Phe
  • NP_001395414.1:p.Leu373Phe
  • NP_001395418.1:p.Leu373Phe
  • NP_001395419.1:p.Leu373Phe
  • NP_001395420.1:p.Leu373Phe
  • NP_001395421.1:p.Leu372Phe
  • NP_001395422.1:p.Leu372Phe
  • NP_001395423.1:p.Leu364Phe
  • NP_001395424.1:p.Leu362Phe
  • NP_001395425.1:p.Leu356Phe
  • NP_001395426.1:p.Leu356Phe
  • NP_001395427.1:p.Leu356Phe
  • NP_001395428.1:p.Leu356Phe
  • NP_001395429.1:p.Leu356Phe
  • NP_001395430.1:p.Leu356Phe
  • NP_001395431.1:p.Leu355Phe
  • NP_001395432.1:p.Leu355Phe
  • NP_001395433.1:p.Leu355Phe
  • NP_001395434.1:p.Leu354Phe
  • NP_001395435.1:p.Leu335Phe
  • NP_001395436.1:p.Leu334Phe
  • NP_001395437.1:p.Leu331Phe
  • NP_001395438.1:p.Leu330Phe
  • NP_001395439.1:p.Leu317Phe
  • NP_001395440.1:p.Leu316Phe
  • NP_001395441.1:p.Leu276Phe
  • NP_009225.1:p.Leu1547Phe
  • NP_009225.1:p.Leu1547Phe
  • NP_009228.2:p.Leu1500Phe
  • NP_009229.2:p.Leu443Phe
  • NP_009229.2:p.Leu443Phe
  • NP_009230.2:p.Leu443Phe
  • NP_009231.2:p.Leu1568Phe
  • NP_009235.2:p.Leu443Phe
  • LRG_292t1:c.4641G>T
  • LRG_292:g.143619G>T
  • LRG_292p1:p.Leu1547Phe
  • NC_000017.10:g.41226382C>A
  • NM_007294.3:c.4641G>T
  • NM_007298.3:c.1329G>T
  • NR_027676.2:n.4818G>T
Protein change:
L1250F
Links:
dbSNP: rs864622265
NCBI 1000 Genomes Browser:
rs864622265
Molecular consequence:
  • NM_001407571.1:c.4428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407581.1:c.4707G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.4707G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.4704G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.4704G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.4704G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.4701G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.4701G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.4641G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.4641G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.4641G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.4641G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.4641G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.4641G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.4641G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.4641G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.4632G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.4632G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.4629G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.4626G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.4584G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.4581G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.4641G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.4563G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.4563G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.4563G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.4560G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.4560G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.4560G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.4557G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.4557G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.4557G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.4557G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.4557G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.4518G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.4518G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.4518G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.4518G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.4518G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.4518G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.4515G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.4515G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.4515G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.4515G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.4515G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.4515G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.4515G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.4515G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.4515G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.4515G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.4515G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.4512G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.4512G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.4512G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.4641G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.4512G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.4512G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.4512G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.4512G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.4512G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.4509G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.4509G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407692.1:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407694.1:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407695.1:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407696.1:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407697.1:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407698.1:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407724.1:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407725.1:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407726.1:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407727.1:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407728.1:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407729.1:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407730.1:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407731.1:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407732.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407733.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407734.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407735.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407736.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407737.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407738.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407739.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407740.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407741.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407742.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407743.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407744.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407745.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407746.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407747.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407748.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407749.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407750.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407751.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407752.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407838.1:c.4494G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407839.1:c.4494G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407841.1:c.4494G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407842.1:c.4494G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407843.1:c.4494G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407844.1:c.4494G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407845.1:c.4494G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407846.1:c.4494G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407847.1:c.4494G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407848.1:c.4494G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407849.1:c.4494G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407850.1:c.4494G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407851.1:c.4494G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407852.1:c.4494G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407853.1:c.4494G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.4641G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407858.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407859.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.4638G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407861.1:c.4635G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.4440G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.4515G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.4434G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.4434G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407879.1:c.4431G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407881.1:c.4431G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407882.1:c.4431G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407884.1:c.4431G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407885.1:c.4431G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407886.1:c.4431G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407887.1:c.4431G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407889.1:c.4431G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407894.1:c.4428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407895.1:c.4428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407896.1:c.4428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407897.1:c.4428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407898.1:c.4428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407899.1:c.4428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407900.1:c.4428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407902.1:c.4428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407904.1:c.4428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407906.1:c.4428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407907.1:c.4428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407908.1:c.4428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407909.1:c.4428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407910.1:c.4428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407915.1:c.4425G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407916.1:c.4425G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407917.1:c.4425G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407918.1:c.4425G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.4518G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407920.1:c.4377G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407921.1:c.4377G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407922.1:c.4377G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407923.1:c.4377G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407924.1:c.4377G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407925.1:c.4377G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407926.1:c.4377G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407927.1:c.4374G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407928.1:c.4374G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407929.1:c.4374G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407930.1:c.4374G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407931.1:c.4374G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407932.1:c.4374G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407933.1:c.4374G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407934.1:c.4371G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407935.1:c.4371G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407936.1:c.4371G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.4518G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.4518G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407939.1:c.4515G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.4515G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407941.1:c.4512G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407942.1:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407943.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407944.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407945.1:c.4497G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407946.1:c.4308G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407947.1:c.4308G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407948.1:c.4308G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407949.1:c.4308G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407950.1:c.4305G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407951.1:c.4305G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407952.1:c.4305G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407953.1:c.4305G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407954.1:c.4305G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407955.1:c.4305G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407956.1:c.4302G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407957.1:c.4302G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407958.1:c.4302G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407959.1:c.4260G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407960.1:c.4257G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407962.1:c.4257G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407963.1:c.4254G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407965.1:c.4134G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407966.1:c.3753G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407967.1:c.3750G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407968.1:c.2037G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407969.1:c.2034G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407970.1:c.1398G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407971.1:c.1398G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407972.1:c.1395G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407973.1:c.1332G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407974.1:c.1332G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407975.1:c.1332G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407976.1:c.1332G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407977.1:c.1332G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407978.1:c.1332G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407979.1:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407980.1:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407981.1:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407982.1:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407983.1:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407984.1:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407985.1:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407986.1:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407990.1:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407991.1:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407992.1:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407993.1:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408392.1:c.1326G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408396.1:c.1326G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408397.1:c.1326G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408398.1:c.1326G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408399.1:c.1326G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408400.1:c.1326G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408401.1:c.1326G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408402.1:c.1326G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408403.1:c.1326G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408404.1:c.1326G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408406.1:c.1323G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408407.1:c.1323G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408408.1:c.1323G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408409.1:c.1320G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408410.1:c.1257G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408411.1:c.1254G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408412.1:c.1251G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408413.1:c.1251G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408414.1:c.1251G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408415.1:c.1251G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408416.1:c.1251G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408418.1:c.1215G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408419.1:c.1215G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408420.1:c.1215G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408421.1:c.1212G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408422.1:c.1212G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408423.1:c.1212G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408424.1:c.1212G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408425.1:c.1209G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408426.1:c.1209G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408427.1:c.1209G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408428.1:c.1209G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408429.1:c.1209G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408430.1:c.1209G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408431.1:c.1209G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408432.1:c.1206G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408433.1:c.1206G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408434.1:c.1206G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408435.1:c.1206G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408436.1:c.1206G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408437.1:c.1206G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408438.1:c.1206G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408439.1:c.1206G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408440.1:c.1206G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408441.1:c.1206G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408442.1:c.1206G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408443.1:c.1206G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408444.1:c.1206G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408445.1:c.1203G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408446.1:c.1203G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408447.1:c.1203G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408448.1:c.1203G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408450.1:c.1203G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408451.1:c.1197G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408452.1:c.1191G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408453.1:c.1191G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408454.1:c.1191G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408455.1:c.1191G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408456.1:c.1191G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408457.1:c.1191G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408458.1:c.1188G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408459.1:c.1188G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408460.1:c.1188G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408461.1:c.1188G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408462.1:c.1188G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408463.1:c.1188G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408464.1:c.1188G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408465.1:c.1188G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408466.1:c.1188G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408467.1:c.1188G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408468.1:c.1185G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408469.1:c.1185G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408470.1:c.1185G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408472.1:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408473.1:c.1326G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408474.1:c.1131G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408475.1:c.1128G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408476.1:c.1128G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408478.1:c.1122G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408479.1:c.1122G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408480.1:c.1122G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408481.1:c.1119G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408482.1:c.1119G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408483.1:c.1119G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408484.1:c.1119G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408485.1:c.1119G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408489.1:c.1119G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408490.1:c.1119G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408491.1:c.1119G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408492.1:c.1116G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408493.1:c.1116G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408494.1:c.1092G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408495.1:c.1086G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408496.1:c.1068G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408497.1:c.1068G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408498.1:c.1068G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408499.1:c.1068G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408500.1:c.1068G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408501.1:c.1068G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408502.1:c.1065G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408503.1:c.1065G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408504.1:c.1065G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408505.1:c.1062G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408506.1:c.1005G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408507.1:c.1002G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408508.1:c.993G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408509.1:c.990G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408510.1:c.951G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408511.1:c.948G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408512.1:c.828G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.4641G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007297.4:c.4500G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007298.4:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007299.4:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.4704G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007304.2:c.1329G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NR_027676.2:n.4818G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Hereditary breast ovarian cancer syndrome
Synonyms:
Hereditary breast and ovarian cancer syndrome; Hereditary breast and ovarian cancer; Hereditary breast and ovarian cancer syndrome (HBOC); See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0003582; MeSH: D061325; MedGen: C0677776; Orphanet: 145

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000259902Invitae
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))
Uncertain significance
(Dec 7, 2016)
germlineclinical testing

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

Summary from all submissions

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Invitae, SCV000259902.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

In summary, this variant is a novel missense change that is not predicted to affect protein function. There is no indication that it causes disease, but the available evidence is currently insufficient to prove that conclusively. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function output the following: (SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0"). The phenylalanine amino acid residue is found in multiple mammalian species, suggesting that this missense change does not adversely affect protein function. These predictions have not been confirmed by published functional studies. This variant is not present in population databases (ExAC no frequency) and has not been reported in the literature in individuals with a BRCA1-related disease. This sequence change replaces leucine with phenylalanine at codon 1547 of the BRCA1 protein (p.Leu1547Phe). The leucine residue is moderately conserved and there is a small physicochemical difference between leucine and phenylalanine.

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

Last Updated: Jul 15, 2024