ClinVar Miner

List of variants in gene combination LOC102724058, SCN1A reported as likely benign by GeneDx

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Total variants: 65
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HGVS dbSNP
NM_001165963.4(SCN1A):c.3101T>C (p.Ile1034Thr) rs121918818
NM_001165963.4(SCN1A):c.3105A>G (p.Gln1035=) rs144013543
NM_001165963.4(SCN1A):c.3111C>A (p.Ser1037=) rs1204620691
NM_001165963.4(SCN1A):c.3246T>C (p.Thr1082=) rs961517010
NM_001165963.4(SCN1A):c.3249A>C (p.Thr1083=) rs1042252202
NM_001165963.4(SCN1A):c.3387G>A (p.Thr1129=) rs375953445
NM_001165963.4(SCN1A):c.3450C>T (p.Ser1150=) rs727504137
NM_001165963.4(SCN1A):c.3477C>T (p.Ile1159=) rs761878186
NM_001165963.4(SCN1A):c.3480C>A (p.Gly1160=) rs369594817
NM_001165963.4(SCN1A):c.3480C>T (p.Gly1160=) rs369594817
NM_001165963.4(SCN1A):c.3521C>G (p.Thr1174Ser) rs121918799
NM_001165963.4(SCN1A):c.3525T>G (p.Leu1175=) rs1057524122
NM_001165963.4(SCN1A):c.3573T>C (p.Cys1191=) rs750943685
NM_001165963.4(SCN1A):c.3576T>C (p.Cys1192=) rs150638891
NM_001165963.4(SCN1A):c.3585T>C (p.Asn1195=) rs138181528
NM_001165963.4(SCN1A):c.3591A>G (p.Glu1197=) rs371596040
NM_001165963.4(SCN1A):c.3630G>A (p.Thr1210=) rs377326177
NM_001165963.4(SCN1A):c.3638G>A (p.Arg1213Gln) rs566081370
NM_001165963.4(SCN1A):c.3717T>C (p.Asp1239=) rs376579606
NM_001165963.4(SCN1A):c.3741G>A (p.Thr1247=) rs200745708
NM_001165963.4(SCN1A):c.3750G>T (p.Thr1250=) rs771494149
NM_001165963.4(SCN1A):c.3888G>A (p.Leu1296=) rs998325208
NM_001165963.4(SCN1A):c.3924A>T (p.Glu1308Asp) rs121917910
NM_001165963.4(SCN1A):c.4095C>T (p.Gly1365=) rs372749240
NM_001165963.4(SCN1A):c.4167C>T (p.Asp1389=) rs376118833
NM_001165963.4(SCN1A):c.4521C>T (p.Tyr1507=) rs750997506
NM_001165963.4(SCN1A):c.4551A>G (p.Lys1517=) rs374087499
NM_001165963.4(SCN1A):c.4632C>T (p.Asp1544=) rs1057521371
NM_001165963.4(SCN1A):c.4791T>C (p.His1597=) rs141051370
NM_001165963.4(SCN1A):c.4870C>T (p.Leu1624=) rs1553520513
NM_001165963.4(SCN1A):c.4887C>T (p.Phe1629=) rs587780445
NM_001165963.4(SCN1A):c.4905C>T (p.Phe1635=) rs774858072
NM_001165963.4(SCN1A):c.4923T>C (p.Ala1641=) rs369650500
NM_001165963.4(SCN1A):c.4980C>T (p.Leu1660=) rs1057521307
NM_001165963.4(SCN1A):c.5026C>T (p.Leu1676=) rs1553520391
NM_001165963.4(SCN1A):c.5127C>A (p.Thr1709=) rs777044331
NM_001165963.4(SCN1A):c.5217C>T (p.Pro1739=) rs149315236
NM_001165963.4(SCN1A):c.5379T>A (p.Thr1793=) rs1553520152
NM_001165963.4(SCN1A):c.5532A>G (p.Pro1844=) rs886043063
NM_001165963.4(SCN1A):c.5632_5634delinsAAT (p.Glu1878Asn) rs1573944260
NM_001165963.4(SCN1A):c.5656C>A (p.Arg1886=) rs779614747
NM_001165963.4(SCN1A):c.5739A>G (p.Lys1913=) rs554861427
NM_001165963.4(SCN1A):c.5763T>C (p.Ile1921=) rs767698089
NM_001165963.4(SCN1A):c.5782C>G (p.Arg1928Gly) rs121917956
NM_001165963.4(SCN1A):c.5823G>A (p.Thr1941=) rs754371368
NM_001165963.4(SCN1A):c.5865A>G (p.Ile1955Met) rs796052952
NM_001165963.4(SCN1A):c.5977A>G (p.Ile1993Val) rs751750112
NM_006920.6(SCN1A):c.3397-7C>A rs975085305
NM_006920.6(SCN1A):c.3672+17A>G rs1553532428
NM_006920.6(SCN1A):c.3673-146C>G rs115294408
NM_006920.6(SCN1A):c.3673-20G>A rs187973818
NM_006920.6(SCN1A):c.3970-15C>T rs1057521559
NM_006920.6(SCN1A):c.3970-8T>C rs1553525411
NM_006920.6(SCN1A):c.4251+19C>A rs1383995139
NM_006920.6(SCN1A):c.4305+12T>C rs761062999
NM_006920.6(SCN1A):c.4305+17dup rs1064795145
NM_006920.6(SCN1A):c.4306-5G>A rs1057522587
NM_006920.6(SCN1A):c.4443+6T>C rs1057523807
NM_006920.6(SCN1A):c.4444-11C>A rs775315152
NM_006920.6(SCN1A):c.4548+124C>G rs13398882
NM_006920.6(SCN1A):c.4548+12C>T rs886055042
NM_006920.6(SCN1A):c.4549-12A>G rs752455718
NM_006920.6(SCN1A):c.4549-27G>A rs113927395
NM_006920.6(SCN1A):c.4549-4A>C rs1057521695
NM_006920.6(SCN1A):c.4549-4A>G rs1057521695

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