U.S. flag

An official website of the United States government

NM_007294.4(BRCA1):c.4691T>C (p.Leu1564Pro) AND not provided

Germline classification:
Benign (3 submissions)
Last evaluated:
Aug 15, 2021
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:
RCV000587835.22

Allele description [Variation Report for NM_007294.4(BRCA1):c.4691T>C (p.Leu1564Pro)]

NM_007294.4(BRCA1):c.4691T>C (p.Leu1564Pro)

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.4691T>C (p.Leu1564Pro)
Other names:
p.L1564P:CTG>CCG; 4810T>C
HGVS:
  • NC_000017.11:g.43071223A>G
  • NG_005905.2:g.146761T>C
  • NM_001407571.1:c.4478T>C
  • NM_001407581.1:c.4757T>C
  • NM_001407582.1:c.4757T>C
  • NM_001407583.1:c.4754T>C
  • NM_001407585.1:c.4754T>C
  • NM_001407587.1:c.4754T>C
  • NM_001407590.1:c.4751T>C
  • NM_001407591.1:c.4751T>C
  • NM_001407593.1:c.4691T>C
  • NM_001407594.1:c.4691T>C
  • NM_001407596.1:c.4691T>C
  • NM_001407597.1:c.4691T>C
  • NM_001407598.1:c.4691T>C
  • NM_001407602.1:c.4691T>C
  • NM_001407603.1:c.4691T>C
  • NM_001407605.1:c.4691T>C
  • NM_001407610.1:c.4688T>C
  • NM_001407611.1:c.4688T>C
  • NM_001407612.1:c.4688T>C
  • NM_001407613.1:c.4688T>C
  • NM_001407614.1:c.4688T>C
  • NM_001407615.1:c.4688T>C
  • NM_001407616.1:c.4688T>C
  • NM_001407617.1:c.4688T>C
  • NM_001407618.1:c.4688T>C
  • NM_001407619.1:c.4688T>C
  • NM_001407620.1:c.4688T>C
  • NM_001407621.1:c.4688T>C
  • NM_001407622.1:c.4688T>C
  • NM_001407623.1:c.4688T>C
  • NM_001407624.1:c.4688T>C
  • NM_001407625.1:c.4688T>C
  • NM_001407626.1:c.4688T>C
  • NM_001407627.1:c.4685T>C
  • NM_001407628.1:c.4685T>C
  • NM_001407629.1:c.4685T>C
  • NM_001407630.1:c.4685T>C
  • NM_001407631.1:c.4685T>C
  • NM_001407632.1:c.4685T>C
  • NM_001407633.1:c.4685T>C
  • NM_001407634.1:c.4685T>C
  • NM_001407635.1:c.4685T>C
  • NM_001407636.1:c.4685T>C
  • NM_001407637.1:c.4685T>C
  • NM_001407638.1:c.4685T>C
  • NM_001407639.1:c.4685T>C
  • NM_001407640.1:c.4685T>C
  • NM_001407641.1:c.4685T>C
  • NM_001407642.1:c.4685T>C
  • NM_001407644.1:c.4682T>C
  • NM_001407645.1:c.4682T>C
  • NM_001407646.1:c.4679T>C
  • NM_001407647.1:c.4676T>C
  • NM_001407648.1:c.4634T>C
  • NM_001407649.1:c.4631T>C
  • NM_001407652.1:c.4691T>C
  • NM_001407653.1:c.4613T>C
  • NM_001407654.1:c.4613T>C
  • NM_001407655.1:c.4613T>C
  • NM_001407656.1:c.4610T>C
  • NM_001407657.1:c.4610T>C
  • NM_001407658.1:c.4610T>C
  • NM_001407659.1:c.4607T>C
  • NM_001407660.1:c.4607T>C
  • NM_001407661.1:c.4607T>C
  • NM_001407662.1:c.4607T>C
  • NM_001407663.1:c.4607T>C
  • NM_001407664.1:c.4568T>C
  • NM_001407665.1:c.4568T>C
  • NM_001407666.1:c.4568T>C
  • NM_001407667.1:c.4568T>C
  • NM_001407668.1:c.4568T>C
  • NM_001407669.1:c.4568T>C
  • NM_001407670.1:c.4565T>C
  • NM_001407671.1:c.4565T>C
  • NM_001407672.1:c.4565T>C
  • NM_001407673.1:c.4565T>C
  • NM_001407674.1:c.4565T>C
  • NM_001407675.1:c.4565T>C
  • NM_001407676.1:c.4565T>C
  • NM_001407677.1:c.4565T>C
  • NM_001407678.1:c.4565T>C
  • NM_001407679.1:c.4565T>C
  • NM_001407680.1:c.4565T>C
  • NM_001407681.1:c.4562T>C
  • NM_001407682.1:c.4562T>C
  • NM_001407683.1:c.4562T>C
  • NM_001407684.1:c.4691T>C
  • NM_001407685.1:c.4562T>C
  • NM_001407686.1:c.4562T>C
  • NM_001407687.1:c.4562T>C
  • NM_001407688.1:c.4562T>C
  • NM_001407689.1:c.4562T>C
  • NM_001407690.1:c.4559T>C
  • NM_001407691.1:c.4559T>C
  • NM_001407692.1:c.4550T>C
  • NM_001407694.1:c.4550T>C
  • NM_001407695.1:c.4550T>C
  • NM_001407696.1:c.4550T>C
  • NM_001407697.1:c.4550T>C
  • NM_001407698.1:c.4550T>C
  • NM_001407724.1:c.4550T>C
  • NM_001407725.1:c.4550T>C
  • NM_001407726.1:c.4550T>C
  • NM_001407727.1:c.4550T>C
  • NM_001407728.1:c.4550T>C
  • NM_001407729.1:c.4550T>C
  • NM_001407730.1:c.4550T>C
  • NM_001407731.1:c.4550T>C
  • NM_001407732.1:c.4547T>C
  • NM_001407733.1:c.4547T>C
  • NM_001407734.1:c.4547T>C
  • NM_001407735.1:c.4547T>C
  • NM_001407736.1:c.4547T>C
  • NM_001407737.1:c.4547T>C
  • NM_001407738.1:c.4547T>C
  • NM_001407739.1:c.4547T>C
  • NM_001407740.1:c.4547T>C
  • NM_001407741.1:c.4547T>C
  • NM_001407742.1:c.4547T>C
  • NM_001407743.1:c.4547T>C
  • NM_001407744.1:c.4547T>C
  • NM_001407745.1:c.4547T>C
  • NM_001407746.1:c.4547T>C
  • NM_001407747.1:c.4547T>C
  • NM_001407748.1:c.4547T>C
  • NM_001407749.1:c.4547T>C
  • NM_001407750.1:c.4547T>C
  • NM_001407751.1:c.4547T>C
  • NM_001407752.1:c.4547T>C
  • NM_001407838.1:c.4544T>C
  • NM_001407839.1:c.4544T>C
  • NM_001407841.1:c.4544T>C
  • NM_001407842.1:c.4544T>C
  • NM_001407843.1:c.4544T>C
  • NM_001407844.1:c.4544T>C
  • NM_001407845.1:c.4544T>C
  • NM_001407846.1:c.4544T>C
  • NM_001407847.1:c.4544T>C
  • NM_001407848.1:c.4544T>C
  • NM_001407849.1:c.4544T>C
  • NM_001407850.1:c.4544T>C
  • NM_001407851.1:c.4544T>C
  • NM_001407852.1:c.4544T>C
  • NM_001407853.1:c.4544T>C
  • NM_001407854.1:c.4691T>C
  • NM_001407858.1:c.4688T>C
  • NM_001407859.1:c.4688T>C
  • NM_001407860.1:c.4688T>C
  • NM_001407861.1:c.4685T>C
  • NM_001407862.1:c.4490T>C
  • NM_001407863.1:c.4565T>C
  • NM_001407874.1:c.4484T>C
  • NM_001407875.1:c.4484T>C
  • NM_001407879.1:c.4481T>C
  • NM_001407881.1:c.4481T>C
  • NM_001407882.1:c.4481T>C
  • NM_001407884.1:c.4481T>C
  • NM_001407885.1:c.4481T>C
  • NM_001407886.1:c.4481T>C
  • NM_001407887.1:c.4481T>C
  • NM_001407889.1:c.4481T>C
  • NM_001407894.1:c.4478T>C
  • NM_001407895.1:c.4478T>C
  • NM_001407896.1:c.4478T>C
  • NM_001407897.1:c.4478T>C
  • NM_001407898.1:c.4478T>C
  • NM_001407899.1:c.4478T>C
  • NM_001407900.1:c.4478T>C
  • NM_001407902.1:c.4478T>C
  • NM_001407904.1:c.4478T>C
  • NM_001407906.1:c.4478T>C
  • NM_001407907.1:c.4478T>C
  • NM_001407908.1:c.4478T>C
  • NM_001407909.1:c.4478T>C
  • NM_001407910.1:c.4478T>C
  • NM_001407915.1:c.4475T>C
  • NM_001407916.1:c.4475T>C
  • NM_001407917.1:c.4475T>C
  • NM_001407918.1:c.4475T>C
  • NM_001407919.1:c.4568T>C
  • NM_001407920.1:c.4427T>C
  • NM_001407921.1:c.4427T>C
  • NM_001407922.1:c.4427T>C
  • NM_001407923.1:c.4427T>C
  • NM_001407924.1:c.4427T>C
  • NM_001407925.1:c.4427T>C
  • NM_001407926.1:c.4427T>C
  • NM_001407927.1:c.4424T>C
  • NM_001407928.1:c.4424T>C
  • NM_001407929.1:c.4424T>C
  • NM_001407930.1:c.4424T>C
  • NM_001407931.1:c.4424T>C
  • NM_001407932.1:c.4424T>C
  • NM_001407933.1:c.4424T>C
  • NM_001407934.1:c.4421T>C
  • NM_001407935.1:c.4421T>C
  • NM_001407936.1:c.4421T>C
  • NM_001407937.1:c.4568T>C
  • NM_001407938.1:c.4568T>C
  • NM_001407939.1:c.4565T>C
  • NM_001407940.1:c.4565T>C
  • NM_001407941.1:c.4562T>C
  • NM_001407942.1:c.4550T>C
  • NM_001407943.1:c.4547T>C
  • NM_001407944.1:c.4547T>C
  • NM_001407945.1:c.4547T>C
  • NM_001407946.1:c.4358T>C
  • NM_001407947.1:c.4358T>C
  • NM_001407948.1:c.4358T>C
  • NM_001407949.1:c.4358T>C
  • NM_001407950.1:c.4355T>C
  • NM_001407951.1:c.4355T>C
  • NM_001407952.1:c.4355T>C
  • NM_001407953.1:c.4355T>C
  • NM_001407954.1:c.4355T>C
  • NM_001407955.1:c.4355T>C
  • NM_001407956.1:c.4352T>C
  • NM_001407957.1:c.4352T>C
  • NM_001407958.1:c.4352T>C
  • NM_001407959.1:c.4310T>C
  • NM_001407960.1:c.4307T>C
  • NM_001407962.1:c.4307T>C
  • NM_001407963.1:c.4304T>C
  • NM_001407964.1:c.4229T>C
  • NM_001407965.1:c.4184T>C
  • NM_001407966.1:c.3803T>C
  • NM_001407967.1:c.3800T>C
  • NM_001407968.1:c.2087T>C
  • NM_001407969.1:c.2084T>C
  • NM_001407970.1:c.1448T>C
  • NM_001407971.1:c.1448T>C
  • NM_001407972.1:c.1445T>C
  • NM_001407973.1:c.1382T>C
  • NM_001407974.1:c.1382T>C
  • NM_001407975.1:c.1382T>C
  • NM_001407976.1:c.1382T>C
  • NM_001407977.1:c.1382T>C
  • NM_001407978.1:c.1382T>C
  • NM_001407979.1:c.1379T>C
  • NM_001407980.1:c.1379T>C
  • NM_001407981.1:c.1379T>C
  • NM_001407982.1:c.1379T>C
  • NM_001407983.1:c.1379T>C
  • NM_001407984.1:c.1379T>C
  • NM_001407985.1:c.1379T>C
  • NM_001407986.1:c.1379T>C
  • NM_001407990.1:c.1379T>C
  • NM_001407991.1:c.1379T>C
  • NM_001407992.1:c.1379T>C
  • NM_001407993.1:c.1379T>C
  • NM_001408392.1:c.1376T>C
  • NM_001408396.1:c.1376T>C
  • NM_001408397.1:c.1376T>C
  • NM_001408398.1:c.1376T>C
  • NM_001408399.1:c.1376T>C
  • NM_001408400.1:c.1376T>C
  • NM_001408401.1:c.1376T>C
  • NM_001408402.1:c.1376T>C
  • NM_001408403.1:c.1376T>C
  • NM_001408404.1:c.1376T>C
  • NM_001408406.1:c.1373T>C
  • NM_001408407.1:c.1373T>C
  • NM_001408408.1:c.1373T>C
  • NM_001408409.1:c.1370T>C
  • NM_001408410.1:c.1307T>C
  • NM_001408411.1:c.1304T>C
  • NM_001408412.1:c.1301T>C
  • NM_001408413.1:c.1301T>C
  • NM_001408414.1:c.1301T>C
  • NM_001408415.1:c.1301T>C
  • NM_001408416.1:c.1301T>C
  • NM_001408418.1:c.1265T>C
  • NM_001408419.1:c.1265T>C
  • NM_001408420.1:c.1265T>C
  • NM_001408421.1:c.1262T>C
  • NM_001408422.1:c.1262T>C
  • NM_001408423.1:c.1262T>C
  • NM_001408424.1:c.1262T>C
  • NM_001408425.1:c.1259T>C
  • NM_001408426.1:c.1259T>C
  • NM_001408427.1:c.1259T>C
  • NM_001408428.1:c.1259T>C
  • NM_001408429.1:c.1259T>C
  • NM_001408430.1:c.1259T>C
  • NM_001408431.1:c.1259T>C
  • NM_001408432.1:c.1256T>C
  • NM_001408433.1:c.1256T>C
  • NM_001408434.1:c.1256T>C
  • NM_001408435.1:c.1256T>C
  • NM_001408436.1:c.1256T>C
  • NM_001408437.1:c.1256T>C
  • NM_001408438.1:c.1256T>C
  • NM_001408439.1:c.1256T>C
  • NM_001408440.1:c.1256T>C
  • NM_001408441.1:c.1256T>C
  • NM_001408442.1:c.1256T>C
  • NM_001408443.1:c.1256T>C
  • NM_001408444.1:c.1256T>C
  • NM_001408445.1:c.1253T>C
  • NM_001408446.1:c.1253T>C
  • NM_001408447.1:c.1253T>C
  • NM_001408448.1:c.1253T>C
  • NM_001408450.1:c.1253T>C
  • NM_001408451.1:c.1247T>C
  • NM_001408452.1:c.1241T>C
  • NM_001408453.1:c.1241T>C
  • NM_001408454.1:c.1241T>C
  • NM_001408455.1:c.1241T>C
  • NM_001408456.1:c.1241T>C
  • NM_001408457.1:c.1241T>C
  • NM_001408458.1:c.1238T>C
  • NM_001408459.1:c.1238T>C
  • NM_001408460.1:c.1238T>C
  • NM_001408461.1:c.1238T>C
  • NM_001408462.1:c.1238T>C
  • NM_001408463.1:c.1238T>C
  • NM_001408464.1:c.1238T>C
  • NM_001408465.1:c.1238T>C
  • NM_001408466.1:c.1238T>C
  • NM_001408467.1:c.1238T>C
  • NM_001408468.1:c.1235T>C
  • NM_001408469.1:c.1235T>C
  • NM_001408470.1:c.1235T>C
  • NM_001408472.1:c.1379T>C
  • NM_001408473.1:c.1376T>C
  • NM_001408474.1:c.1181T>C
  • NM_001408475.1:c.1178T>C
  • NM_001408476.1:c.1178T>C
  • NM_001408478.1:c.1172T>C
  • NM_001408479.1:c.1172T>C
  • NM_001408480.1:c.1172T>C
  • NM_001408481.1:c.1169T>C
  • NM_001408482.1:c.1169T>C
  • NM_001408483.1:c.1169T>C
  • NM_001408484.1:c.1169T>C
  • NM_001408485.1:c.1169T>C
  • NM_001408489.1:c.1169T>C
  • NM_001408490.1:c.1169T>C
  • NM_001408491.1:c.1169T>C
  • NM_001408492.1:c.1166T>C
  • NM_001408493.1:c.1166T>C
  • NM_001408494.1:c.1142T>C
  • NM_001408495.1:c.1136T>C
  • NM_001408496.1:c.1118T>C
  • NM_001408497.1:c.1118T>C
  • NM_001408498.1:c.1118T>C
  • NM_001408499.1:c.1118T>C
  • NM_001408500.1:c.1118T>C
  • NM_001408501.1:c.1118T>C
  • NM_001408502.1:c.1115T>C
  • NM_001408503.1:c.1115T>C
  • NM_001408504.1:c.1115T>C
  • NM_001408505.1:c.1112T>C
  • NM_001408506.1:c.1055T>C
  • NM_001408507.1:c.1052T>C
  • NM_001408508.1:c.1043T>C
  • NM_001408509.1:c.1040T>C
  • NM_001408510.1:c.1001T>C
  • NM_001408511.1:c.998T>C
  • NM_001408512.1:c.878T>C
  • NM_001408513.1:c.851T>C
  • NM_007294.4:c.4691T>CMANE SELECT
  • NM_007297.4:c.4550T>C
  • NM_007298.4:c.1379T>C
  • NM_007299.4:c.1379T>C
  • NM_007300.4:c.4754T>C
  • NM_007304.2:c.1379T>C
  • NP_001394500.1:p.Leu1493Pro
  • NP_001394510.1:p.Leu1586Pro
  • NP_001394511.1:p.Leu1586Pro
  • NP_001394512.1:p.Leu1585Pro
  • NP_001394514.1:p.Leu1585Pro
  • NP_001394516.1:p.Leu1585Pro
  • NP_001394519.1:p.Leu1584Pro
  • NP_001394520.1:p.Leu1584Pro
  • NP_001394522.1:p.Leu1564Pro
  • NP_001394523.1:p.Leu1564Pro
  • NP_001394525.1:p.Leu1564Pro
  • NP_001394526.1:p.Leu1564Pro
  • NP_001394527.1:p.Leu1564Pro
  • NP_001394531.1:p.Leu1564Pro
  • NP_001394532.1:p.Leu1564Pro
  • NP_001394534.1:p.Leu1564Pro
  • NP_001394539.1:p.Leu1563Pro
  • NP_001394540.1:p.Leu1563Pro
  • NP_001394541.1:p.Leu1563Pro
  • NP_001394542.1:p.Leu1563Pro
  • NP_001394543.1:p.Leu1563Pro
  • NP_001394544.1:p.Leu1563Pro
  • NP_001394545.1:p.Leu1563Pro
  • NP_001394546.1:p.Leu1563Pro
  • NP_001394547.1:p.Leu1563Pro
  • NP_001394548.1:p.Leu1563Pro
  • NP_001394549.1:p.Leu1563Pro
  • NP_001394550.1:p.Leu1563Pro
  • NP_001394551.1:p.Leu1563Pro
  • NP_001394552.1:p.Leu1563Pro
  • NP_001394553.1:p.Leu1563Pro
  • NP_001394554.1:p.Leu1563Pro
  • NP_001394555.1:p.Leu1563Pro
  • NP_001394556.1:p.Leu1562Pro
  • NP_001394557.1:p.Leu1562Pro
  • NP_001394558.1:p.Leu1562Pro
  • NP_001394559.1:p.Leu1562Pro
  • NP_001394560.1:p.Leu1562Pro
  • NP_001394561.1:p.Leu1562Pro
  • NP_001394562.1:p.Leu1562Pro
  • NP_001394563.1:p.Leu1562Pro
  • NP_001394564.1:p.Leu1562Pro
  • NP_001394565.1:p.Leu1562Pro
  • NP_001394566.1:p.Leu1562Pro
  • NP_001394567.1:p.Leu1562Pro
  • NP_001394568.1:p.Leu1562Pro
  • NP_001394569.1:p.Leu1562Pro
  • NP_001394570.1:p.Leu1562Pro
  • NP_001394571.1:p.Leu1562Pro
  • NP_001394573.1:p.Leu1561Pro
  • NP_001394574.1:p.Leu1561Pro
  • NP_001394575.1:p.Leu1560Pro
  • NP_001394576.1:p.Leu1559Pro
  • NP_001394577.1:p.Leu1545Pro
  • NP_001394578.1:p.Leu1544Pro
  • NP_001394581.1:p.Leu1564Pro
  • NP_001394582.1:p.Leu1538Pro
  • NP_001394583.1:p.Leu1538Pro
  • NP_001394584.1:p.Leu1538Pro
  • NP_001394585.1:p.Leu1537Pro
  • NP_001394586.1:p.Leu1537Pro
  • NP_001394587.1:p.Leu1537Pro
  • NP_001394588.1:p.Leu1536Pro
  • NP_001394589.1:p.Leu1536Pro
  • NP_001394590.1:p.Leu1536Pro
  • NP_001394591.1:p.Leu1536Pro
  • NP_001394592.1:p.Leu1536Pro
  • NP_001394593.1:p.Leu1523Pro
  • NP_001394594.1:p.Leu1523Pro
  • NP_001394595.1:p.Leu1523Pro
  • NP_001394596.1:p.Leu1523Pro
  • NP_001394597.1:p.Leu1523Pro
  • NP_001394598.1:p.Leu1523Pro
  • NP_001394599.1:p.Leu1522Pro
  • NP_001394600.1:p.Leu1522Pro
  • NP_001394601.1:p.Leu1522Pro
  • NP_001394602.1:p.Leu1522Pro
  • NP_001394603.1:p.Leu1522Pro
  • NP_001394604.1:p.Leu1522Pro
  • NP_001394605.1:p.Leu1522Pro
  • NP_001394606.1:p.Leu1522Pro
  • NP_001394607.1:p.Leu1522Pro
  • NP_001394608.1:p.Leu1522Pro
  • NP_001394609.1:p.Leu1522Pro
  • NP_001394610.1:p.Leu1521Pro
  • NP_001394611.1:p.Leu1521Pro
  • NP_001394612.1:p.Leu1521Pro
  • NP_001394613.1:p.Leu1564Pro
  • NP_001394614.1:p.Leu1521Pro
  • NP_001394615.1:p.Leu1521Pro
  • NP_001394616.1:p.Leu1521Pro
  • NP_001394617.1:p.Leu1521Pro
  • NP_001394618.1:p.Leu1521Pro
  • NP_001394619.1:p.Leu1520Pro
  • NP_001394620.1:p.Leu1520Pro
  • NP_001394621.1:p.Leu1517Pro
  • NP_001394623.1:p.Leu1517Pro
  • NP_001394624.1:p.Leu1517Pro
  • NP_001394625.1:p.Leu1517Pro
  • NP_001394626.1:p.Leu1517Pro
  • NP_001394627.1:p.Leu1517Pro
  • NP_001394653.1:p.Leu1517Pro
  • NP_001394654.1:p.Leu1517Pro
  • NP_001394655.1:p.Leu1517Pro
  • NP_001394656.1:p.Leu1517Pro
  • NP_001394657.1:p.Leu1517Pro
  • NP_001394658.1:p.Leu1517Pro
  • NP_001394659.1:p.Leu1517Pro
  • NP_001394660.1:p.Leu1517Pro
  • NP_001394661.1:p.Leu1516Pro
  • NP_001394662.1:p.Leu1516Pro
  • NP_001394663.1:p.Leu1516Pro
  • NP_001394664.1:p.Leu1516Pro
  • NP_001394665.1:p.Leu1516Pro
  • NP_001394666.1:p.Leu1516Pro
  • NP_001394667.1:p.Leu1516Pro
  • NP_001394668.1:p.Leu1516Pro
  • NP_001394669.1:p.Leu1516Pro
  • NP_001394670.1:p.Leu1516Pro
  • NP_001394671.1:p.Leu1516Pro
  • NP_001394672.1:p.Leu1516Pro
  • NP_001394673.1:p.Leu1516Pro
  • NP_001394674.1:p.Leu1516Pro
  • NP_001394675.1:p.Leu1516Pro
  • NP_001394676.1:p.Leu1516Pro
  • NP_001394677.1:p.Leu1516Pro
  • NP_001394678.1:p.Leu1516Pro
  • NP_001394679.1:p.Leu1516Pro
  • NP_001394680.1:p.Leu1516Pro
  • NP_001394681.1:p.Leu1516Pro
  • NP_001394767.1:p.Leu1515Pro
  • NP_001394768.1:p.Leu1515Pro
  • NP_001394770.1:p.Leu1515Pro
  • NP_001394771.1:p.Leu1515Pro
  • NP_001394772.1:p.Leu1515Pro
  • NP_001394773.1:p.Leu1515Pro
  • NP_001394774.1:p.Leu1515Pro
  • NP_001394775.1:p.Leu1515Pro
  • NP_001394776.1:p.Leu1515Pro
  • NP_001394777.1:p.Leu1515Pro
  • NP_001394778.1:p.Leu1515Pro
  • NP_001394779.1:p.Leu1515Pro
  • NP_001394780.1:p.Leu1515Pro
  • NP_001394781.1:p.Leu1515Pro
  • NP_001394782.1:p.Leu1515Pro
  • NP_001394783.1:p.Leu1564Pro
  • NP_001394787.1:p.Leu1563Pro
  • NP_001394788.1:p.Leu1563Pro
  • NP_001394789.1:p.Leu1563Pro
  • NP_001394790.1:p.Leu1562Pro
  • NP_001394791.1:p.Leu1497Pro
  • NP_001394792.1:p.Leu1522Pro
  • NP_001394803.1:p.Leu1495Pro
  • NP_001394804.1:p.Leu1495Pro
  • NP_001394808.1:p.Leu1494Pro
  • NP_001394810.1:p.Leu1494Pro
  • NP_001394811.1:p.Leu1494Pro
  • NP_001394813.1:p.Leu1494Pro
  • NP_001394814.1:p.Leu1494Pro
  • NP_001394815.1:p.Leu1494Pro
  • NP_001394816.1:p.Leu1494Pro
  • NP_001394818.1:p.Leu1494Pro
  • NP_001394823.1:p.Leu1493Pro
  • NP_001394824.1:p.Leu1493Pro
  • NP_001394825.1:p.Leu1493Pro
  • NP_001394826.1:p.Leu1493Pro
  • NP_001394827.1:p.Leu1493Pro
  • NP_001394828.1:p.Leu1493Pro
  • NP_001394829.1:p.Leu1493Pro
  • NP_001394831.1:p.Leu1493Pro
  • NP_001394833.1:p.Leu1493Pro
  • NP_001394835.1:p.Leu1493Pro
  • NP_001394836.1:p.Leu1493Pro
  • NP_001394837.1:p.Leu1493Pro
  • NP_001394838.1:p.Leu1493Pro
  • NP_001394839.1:p.Leu1493Pro
  • NP_001394844.1:p.Leu1492Pro
  • NP_001394845.1:p.Leu1492Pro
  • NP_001394846.1:p.Leu1492Pro
  • NP_001394847.1:p.Leu1492Pro
  • NP_001394848.1:p.Leu1523Pro
  • NP_001394849.1:p.Leu1476Pro
  • NP_001394850.1:p.Leu1476Pro
  • NP_001394851.1:p.Leu1476Pro
  • NP_001394852.1:p.Leu1476Pro
  • NP_001394853.1:p.Leu1476Pro
  • NP_001394854.1:p.Leu1476Pro
  • NP_001394855.1:p.Leu1476Pro
  • NP_001394856.1:p.Leu1475Pro
  • NP_001394857.1:p.Leu1475Pro
  • NP_001394858.1:p.Leu1475Pro
  • NP_001394859.1:p.Leu1475Pro
  • NP_001394860.1:p.Leu1475Pro
  • NP_001394861.1:p.Leu1475Pro
  • NP_001394862.1:p.Leu1475Pro
  • NP_001394863.1:p.Leu1474Pro
  • NP_001394864.1:p.Leu1474Pro
  • NP_001394865.1:p.Leu1474Pro
  • NP_001394866.1:p.Leu1523Pro
  • NP_001394867.1:p.Leu1523Pro
  • NP_001394868.1:p.Leu1522Pro
  • NP_001394869.1:p.Leu1522Pro
  • NP_001394870.1:p.Leu1521Pro
  • NP_001394871.1:p.Leu1517Pro
  • NP_001394872.1:p.Leu1516Pro
  • NP_001394873.1:p.Leu1516Pro
  • NP_001394874.1:p.Leu1516Pro
  • NP_001394875.1:p.Leu1453Pro
  • NP_001394876.1:p.Leu1453Pro
  • NP_001394877.1:p.Leu1453Pro
  • NP_001394878.1:p.Leu1453Pro
  • NP_001394879.1:p.Leu1452Pro
  • NP_001394880.1:p.Leu1452Pro
  • NP_001394881.1:p.Leu1452Pro
  • NP_001394882.1:p.Leu1452Pro
  • NP_001394883.1:p.Leu1452Pro
  • NP_001394884.1:p.Leu1452Pro
  • NP_001394885.1:p.Leu1451Pro
  • NP_001394886.1:p.Leu1451Pro
  • NP_001394887.1:p.Leu1451Pro
  • NP_001394888.1:p.Leu1437Pro
  • NP_001394889.1:p.Leu1436Pro
  • NP_001394891.1:p.Leu1436Pro
  • NP_001394892.1:p.Leu1435Pro
  • NP_001394893.1:p.Leu1410Pro
  • NP_001394894.1:p.Leu1395Pro
  • NP_001394895.1:p.Leu1268Pro
  • NP_001394896.1:p.Leu1267Pro
  • NP_001394897.1:p.Leu696Pro
  • NP_001394898.1:p.Leu695Pro
  • NP_001394899.1:p.Leu483Pro
  • NP_001394900.1:p.Leu483Pro
  • NP_001394901.1:p.Leu482Pro
  • NP_001394902.1:p.Leu461Pro
  • NP_001394903.1:p.Leu461Pro
  • NP_001394904.1:p.Leu461Pro
  • NP_001394905.1:p.Leu461Pro
  • NP_001394906.1:p.Leu461Pro
  • NP_001394907.1:p.Leu461Pro
  • NP_001394908.1:p.Leu460Pro
  • NP_001394909.1:p.Leu460Pro
  • NP_001394910.1:p.Leu460Pro
  • NP_001394911.1:p.Leu460Pro
  • NP_001394912.1:p.Leu460Pro
  • NP_001394913.1:p.Leu460Pro
  • NP_001394914.1:p.Leu460Pro
  • NP_001394915.1:p.Leu460Pro
  • NP_001394919.1:p.Leu460Pro
  • NP_001394920.1:p.Leu460Pro
  • NP_001394921.1:p.Leu460Pro
  • NP_001394922.1:p.Leu460Pro
  • NP_001395321.1:p.Leu459Pro
  • NP_001395325.1:p.Leu459Pro
  • NP_001395326.1:p.Leu459Pro
  • NP_001395327.1:p.Leu459Pro
  • NP_001395328.1:p.Leu459Pro
  • NP_001395329.1:p.Leu459Pro
  • NP_001395330.1:p.Leu459Pro
  • NP_001395331.1:p.Leu459Pro
  • NP_001395332.1:p.Leu459Pro
  • NP_001395333.1:p.Leu459Pro
  • NP_001395335.1:p.Leu458Pro
  • NP_001395336.1:p.Leu458Pro
  • NP_001395337.1:p.Leu458Pro
  • NP_001395338.1:p.Leu457Pro
  • NP_001395339.1:p.Leu436Pro
  • NP_001395340.1:p.Leu435Pro
  • NP_001395341.1:p.Leu434Pro
  • NP_001395342.1:p.Leu434Pro
  • NP_001395343.1:p.Leu434Pro
  • NP_001395344.1:p.Leu434Pro
  • NP_001395345.1:p.Leu434Pro
  • NP_001395347.1:p.Leu422Pro
  • NP_001395348.1:p.Leu422Pro
  • NP_001395349.1:p.Leu422Pro
  • NP_001395350.1:p.Leu421Pro
  • NP_001395351.1:p.Leu421Pro
  • NP_001395352.1:p.Leu421Pro
  • NP_001395353.1:p.Leu421Pro
  • NP_001395354.1:p.Leu420Pro
  • NP_001395355.1:p.Leu420Pro
  • NP_001395356.1:p.Leu420Pro
  • NP_001395357.1:p.Leu420Pro
  • NP_001395358.1:p.Leu420Pro
  • NP_001395359.1:p.Leu420Pro
  • NP_001395360.1:p.Leu420Pro
  • NP_001395361.1:p.Leu419Pro
  • NP_001395362.1:p.Leu419Pro
  • NP_001395363.1:p.Leu419Pro
  • NP_001395364.1:p.Leu419Pro
  • NP_001395365.1:p.Leu419Pro
  • NP_001395366.1:p.Leu419Pro
  • NP_001395367.1:p.Leu419Pro
  • NP_001395368.1:p.Leu419Pro
  • NP_001395369.1:p.Leu419Pro
  • NP_001395370.1:p.Leu419Pro
  • NP_001395371.1:p.Leu419Pro
  • NP_001395372.1:p.Leu419Pro
  • NP_001395373.1:p.Leu419Pro
  • NP_001395374.1:p.Leu418Pro
  • NP_001395375.1:p.Leu418Pro
  • NP_001395376.1:p.Leu418Pro
  • NP_001395377.1:p.Leu418Pro
  • NP_001395379.1:p.Leu418Pro
  • NP_001395380.1:p.Leu416Pro
  • NP_001395381.1:p.Leu414Pro
  • NP_001395382.1:p.Leu414Pro
  • NP_001395383.1:p.Leu414Pro
  • NP_001395384.1:p.Leu414Pro
  • NP_001395385.1:p.Leu414Pro
  • NP_001395386.1:p.Leu414Pro
  • NP_001395387.1:p.Leu413Pro
  • NP_001395388.1:p.Leu413Pro
  • NP_001395389.1:p.Leu413Pro
  • NP_001395390.1:p.Leu413Pro
  • NP_001395391.1:p.Leu413Pro
  • NP_001395392.1:p.Leu413Pro
  • NP_001395393.1:p.Leu413Pro
  • NP_001395394.1:p.Leu413Pro
  • NP_001395395.1:p.Leu413Pro
  • NP_001395396.1:p.Leu413Pro
  • NP_001395397.1:p.Leu412Pro
  • NP_001395398.1:p.Leu412Pro
  • NP_001395399.1:p.Leu412Pro
  • NP_001395401.1:p.Leu460Pro
  • NP_001395402.1:p.Leu459Pro
  • NP_001395403.1:p.Leu394Pro
  • NP_001395404.1:p.Leu393Pro
  • NP_001395405.1:p.Leu393Pro
  • NP_001395407.1:p.Leu391Pro
  • NP_001395408.1:p.Leu391Pro
  • NP_001395409.1:p.Leu391Pro
  • NP_001395410.1:p.Leu390Pro
  • NP_001395411.1:p.Leu390Pro
  • NP_001395412.1:p.Leu390Pro
  • NP_001395413.1:p.Leu390Pro
  • NP_001395414.1:p.Leu390Pro
  • NP_001395418.1:p.Leu390Pro
  • NP_001395419.1:p.Leu390Pro
  • NP_001395420.1:p.Leu390Pro
  • NP_001395421.1:p.Leu389Pro
  • NP_001395422.1:p.Leu389Pro
  • NP_001395423.1:p.Leu381Pro
  • NP_001395424.1:p.Leu379Pro
  • NP_001395425.1:p.Leu373Pro
  • NP_001395426.1:p.Leu373Pro
  • NP_001395427.1:p.Leu373Pro
  • NP_001395428.1:p.Leu373Pro
  • NP_001395429.1:p.Leu373Pro
  • NP_001395430.1:p.Leu373Pro
  • NP_001395431.1:p.Leu372Pro
  • NP_001395432.1:p.Leu372Pro
  • NP_001395433.1:p.Leu372Pro
  • NP_001395434.1:p.Leu371Pro
  • NP_001395435.1:p.Leu352Pro
  • NP_001395436.1:p.Leu351Pro
  • NP_001395437.1:p.Leu348Pro
  • NP_001395438.1:p.Leu347Pro
  • NP_001395439.1:p.Leu334Pro
  • NP_001395440.1:p.Leu333Pro
  • NP_001395441.1:p.Leu293Pro
  • NP_001395442.1:p.Leu284Pro
  • NP_009225.1:p.Leu1564Pro
  • NP_009225.1:p.Leu1564Pro
  • NP_009228.2:p.Leu1517Pro
  • NP_009229.2:p.Leu460Pro
  • NP_009229.2:p.Leu460Pro
  • NP_009230.2:p.Leu460Pro
  • NP_009231.2:p.Leu1585Pro
  • NP_009235.2:p.Leu460Pro
  • LRG_292t1:c.4691T>C
  • LRG_292:g.146761T>C
  • LRG_292p1:p.Leu1564Pro
  • NC_000017.10:g.41223240A>G
  • NM_007294.3:c.4691T>C
  • NM_007298.3:c.1379T>C
  • NM_007300.3:c.4754T>C
  • NR_027676.2:n.4868T>C
  • U14680.1:n.4810T>C
  • p.L1564P
Protein change:
L1267P
Links:
BRCA1-HCI: BRCA1_00023; dbSNP: rs56119278
NCBI 1000 Genomes Browser:
rs56119278
Molecular consequence:
  • NM_001407571.1:c.4478T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407581.1:c.4757T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.4757T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.4754T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.4754T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.4754T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.4751T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.4751T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.4691T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.4691T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.4691T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.4691T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.4691T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.4691T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.4691T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.4691T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.4682T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.4682T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.4679T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.4676T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.4634T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.4631T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.4691T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.4613T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.4613T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.4613T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.4610T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.4610T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.4610T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.4607T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.4607T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.4607T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.4607T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.4607T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.4568T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.4568T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.4568T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.4568T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.4568T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.4568T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.4565T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.4565T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.4565T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.4565T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.4565T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.4565T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.4565T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.4565T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.4565T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.4565T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.4565T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.4562T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.4562T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.4562T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.4691T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.4562T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.4562T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.4562T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.4562T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.4562T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.4559T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.4559T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407692.1:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407694.1:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407695.1:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407696.1:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407697.1:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407698.1:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407724.1:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407725.1:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407726.1:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407727.1:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407728.1:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407729.1:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407730.1:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407731.1:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407732.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407733.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407734.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407735.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407736.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407737.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407738.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407739.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407740.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407741.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407742.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407743.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407744.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407745.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407746.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407747.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407748.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407749.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407750.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407751.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407752.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407838.1:c.4544T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407839.1:c.4544T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407841.1:c.4544T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407842.1:c.4544T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407843.1:c.4544T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407844.1:c.4544T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407845.1:c.4544T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407846.1:c.4544T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407847.1:c.4544T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407848.1:c.4544T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407849.1:c.4544T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407850.1:c.4544T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407851.1:c.4544T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407852.1:c.4544T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407853.1:c.4544T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.4691T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407858.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407859.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.4688T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407861.1:c.4685T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.4490T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.4565T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.4484T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.4484T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407879.1:c.4481T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407881.1:c.4481T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407882.1:c.4481T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407884.1:c.4481T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407885.1:c.4481T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407886.1:c.4481T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407887.1:c.4481T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407889.1:c.4481T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407894.1:c.4478T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407895.1:c.4478T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407896.1:c.4478T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407897.1:c.4478T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407898.1:c.4478T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407899.1:c.4478T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407900.1:c.4478T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407902.1:c.4478T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407904.1:c.4478T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407906.1:c.4478T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407907.1:c.4478T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407908.1:c.4478T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407909.1:c.4478T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407910.1:c.4478T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407915.1:c.4475T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407916.1:c.4475T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407917.1:c.4475T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407918.1:c.4475T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.4568T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407920.1:c.4427T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407921.1:c.4427T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407922.1:c.4427T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407923.1:c.4427T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407924.1:c.4427T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407925.1:c.4427T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407926.1:c.4427T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407927.1:c.4424T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407928.1:c.4424T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407929.1:c.4424T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407930.1:c.4424T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407931.1:c.4424T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407932.1:c.4424T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407933.1:c.4424T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407934.1:c.4421T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407935.1:c.4421T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407936.1:c.4421T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.4568T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.4568T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407939.1:c.4565T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.4565T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407941.1:c.4562T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407942.1:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407943.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407944.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407945.1:c.4547T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407946.1:c.4358T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407947.1:c.4358T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407948.1:c.4358T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407949.1:c.4358T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407950.1:c.4355T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407951.1:c.4355T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407952.1:c.4355T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407953.1:c.4355T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407954.1:c.4355T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407955.1:c.4355T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407956.1:c.4352T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407957.1:c.4352T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407958.1:c.4352T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407959.1:c.4310T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407960.1:c.4307T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407962.1:c.4307T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407963.1:c.4304T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407964.1:c.4229T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407965.1:c.4184T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407966.1:c.3803T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407967.1:c.3800T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407968.1:c.2087T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407969.1:c.2084T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407970.1:c.1448T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407971.1:c.1448T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407972.1:c.1445T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407973.1:c.1382T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407974.1:c.1382T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407975.1:c.1382T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407976.1:c.1382T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407977.1:c.1382T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407978.1:c.1382T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407979.1:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407980.1:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407981.1:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407982.1:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407983.1:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407984.1:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407985.1:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407986.1:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407990.1:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407991.1:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407992.1:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407993.1:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408392.1:c.1376T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408396.1:c.1376T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408397.1:c.1376T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408398.1:c.1376T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408399.1:c.1376T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408400.1:c.1376T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408401.1:c.1376T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408402.1:c.1376T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408403.1:c.1376T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408404.1:c.1376T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408406.1:c.1373T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408407.1:c.1373T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408408.1:c.1373T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408409.1:c.1370T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408410.1:c.1307T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408411.1:c.1304T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408412.1:c.1301T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408413.1:c.1301T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408414.1:c.1301T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408415.1:c.1301T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408416.1:c.1301T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408418.1:c.1265T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408419.1:c.1265T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408420.1:c.1265T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408421.1:c.1262T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408422.1:c.1262T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408423.1:c.1262T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408424.1:c.1262T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408425.1:c.1259T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408426.1:c.1259T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408427.1:c.1259T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408428.1:c.1259T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408429.1:c.1259T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408430.1:c.1259T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408431.1:c.1259T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408432.1:c.1256T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408433.1:c.1256T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408434.1:c.1256T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408435.1:c.1256T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408436.1:c.1256T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408437.1:c.1256T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408438.1:c.1256T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408439.1:c.1256T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408440.1:c.1256T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408441.1:c.1256T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408442.1:c.1256T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408443.1:c.1256T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408444.1:c.1256T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408445.1:c.1253T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408446.1:c.1253T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408447.1:c.1253T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408448.1:c.1253T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408450.1:c.1253T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408451.1:c.1247T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408452.1:c.1241T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408453.1:c.1241T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408454.1:c.1241T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408455.1:c.1241T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408456.1:c.1241T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408457.1:c.1241T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408458.1:c.1238T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408459.1:c.1238T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408460.1:c.1238T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408461.1:c.1238T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408462.1:c.1238T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408463.1:c.1238T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408464.1:c.1238T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408465.1:c.1238T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408466.1:c.1238T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408467.1:c.1238T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408468.1:c.1235T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408469.1:c.1235T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408470.1:c.1235T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408472.1:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408473.1:c.1376T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408474.1:c.1181T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408475.1:c.1178T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408476.1:c.1178T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408478.1:c.1172T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408479.1:c.1172T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408480.1:c.1172T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408481.1:c.1169T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408482.1:c.1169T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408483.1:c.1169T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408484.1:c.1169T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408485.1:c.1169T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408489.1:c.1169T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408490.1:c.1169T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408491.1:c.1169T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408492.1:c.1166T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408493.1:c.1166T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408494.1:c.1142T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408495.1:c.1136T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408496.1:c.1118T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408497.1:c.1118T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408498.1:c.1118T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408499.1:c.1118T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408500.1:c.1118T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408501.1:c.1118T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408502.1:c.1115T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408503.1:c.1115T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408504.1:c.1115T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408505.1:c.1112T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408506.1:c.1055T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408507.1:c.1052T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408508.1:c.1043T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408509.1:c.1040T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408510.1:c.1001T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408511.1:c.998T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408512.1:c.878T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408513.1:c.851T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.4691T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007297.4:c.4550T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007298.4:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007299.4:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.4754T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007304.2:c.1379T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NR_027676.2:n.4868T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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
SCV000699165Women's Health and Genetics/Laboratory Corporation of America, LabCorp
criteria provided, single submitter

(LabCorp Variant Classification Summary - May 2015)
Benign
(Mar 17, 2016)
germlineclinical testing

PubMed (16)
[See all records that cite these PMIDs]

LabCorp Variant Classification Summary - May 2015.docx,

Citation Link,

SCV002048592ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories
criteria provided, single submitter

(ARUP Molecular Germline Variant Investigation Process 2021)
Benign
(Aug 15, 2021)
germlineclinical testing

Citation Link,

SCV005251030Breakthrough Genomics, Breakthrough Genomics
criteria provided, single submitter

(ACMG Guidelines, 2015)
Benigngermlinenot provided

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

Summary from all submissions

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

Citations

PubMed

Comprehensive statistical study of 452 BRCA1 missense substitutions with classification of eight recurrent substitutions as neutral.

Tavtigian SV, Deffenbaugh AM, Yin L, Judkins T, Scholl T, Samollow PB, de Silva D, Zharkikh A, Thomas A.

J Med Genet. 2006 Apr;43(4):295-305. Epub 2005 Jul 13.

PubMed [citation]
PMID:
16014699
PMCID:
PMC2563222

Variants of uncertain significance in BRCA1 and BRCA2 assessment of in silico analysis and a proposal for communication in genetic counselling.

Moghadasi S, Hofland N, Wouts JN, Hogervorst FB, Wijnen JT, Vreeswijk MP, van Asperen CJ.

J Med Genet. 2013 Feb;50(2):74-9. doi: 10.1136/jmedgenet-2012-100961. Epub 2012 Dec 11.

PubMed [citation]
PMID:
23231788
See all PubMed Citations (17)

Details of each submission

From Women's Health and Genetics/Laboratory Corporation of America, LabCorp, SCV000699165.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (16)

Description

Variant summary: Variant affects a non-conserved nucleotide and results in a replacement of a medium size and hydrophobic Leucine (L) with a medium size and hydrophobic Proline (P). 3/4 in silico tools predict the variant to be neutral. It was observed predominantly in the African subcohorts of the ExAC project at an allele frequency of 0.13% which slightly exceeds the maximal expected allele frequency of a disease causing BRCA1 allele (0.1%). It was reported in several HBOC spectrum patients however without strong evidence for pathogenicity. The variant was observed to co-occur with pathogenic/possibly pathogenic BRCA1 and BRCA2 variants such as BRCA1 p.C64Y; p.Lys1290Ter, p.Val738fs, c.824ins10 and BRCA2 p.Lys1872_Ile1874fs indicating neutrality. A benign impact is also supported by computational analysis that integrated multiple forms of genetic evidence for the variant of interest (Lindor_2012). Carvalho_2007 showed decreased transcriptional activity in yeast and mammalian cells; however, Hayes_2000 showed transcription activation of the variant is comparable to wild-type BRCA1 in yeast. In addition, multiple literature and reputable databases/clinical laboratories classify this variant as likely benign or benign. Considering all evidence, the variant was classified as Benign.

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

From ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories, SCV002048592.1

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

From Breakthrough Genomics, Breakthrough Genomics, SCV005251030.1

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

Last Updated: Oct 20, 2024