ClinVar Miner

List of variants in gene SCN11A reported as likely benign for not provided

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Gene type:
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Total variants: 82
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HGVS dbSNP gnomAD frequency
NM_001349253.2(SCN11A):c.267+33del rs150760120 0.03497
NM_001349253.2(SCN11A):c.4056+29G>T rs73066579 0.03318
NM_001349253.2(SCN11A):c.267+27del rs765603809 0.01913
NM_001349253.2(SCN11A):c.1299+285C>T rs9848916 0.01509
NM_001349253.2(SCN11A):c.712+62A>G rs114843596 0.01494
NM_001349253.2(SCN11A):c.2023-268C>A rs13315594 0.01437
NM_001349253.2(SCN11A):c.1842+204G>A rs7616269 0.01301
NM_001349253.2(SCN11A):c.617+202T>A rs112060534 0.01196
NM_001349253.2(SCN11A):c.4327+259T>C rs116807211 0.00968
NM_001349253.2(SCN11A):c.3219+245A>G rs115657669 0.00966
NM_001349253.2(SCN11A):c.3220-313A>T rs74783639 0.00966
NM_001349253.2(SCN11A):c.5061C>T (p.Phe1687=) rs75856434 0.00966
NM_001349253.2(SCN11A):c.4056+141C>T rs115396561 0.00965
NM_001349253.2(SCN11A):c.3394-322G>A rs116407170 0.00857
NM_001349253.2(SCN11A):c.267+16G>C rs540729482 0.00718
NM_001349253.2(SCN11A):c.*100C>A rs192005503 0.00600
NM_001349253.2(SCN11A):c.757C>T (p.Leu253=) rs36084747 0.00591
NM_001349253.2(SCN11A):c.268-263C>T rs79087801 0.00571
NM_001349253.2(SCN11A):c.712+55T>A rs75595916 0.00558
NM_001349253.2(SCN11A):c.3064+214G>A rs145262027 0.00543
NM_001349253.2(SCN11A):c.1604-202G>A rs73826402 0.00526
NM_001349253.2(SCN11A):c.712+45T>C rs55689417 0.00525
NM_001349253.2(SCN11A):c.4230G>A (p.Thr1410=) rs78953918 0.00480
NM_001349253.2(SCN11A):c.3952-323G>A rs188158704 0.00472
NM_001349253.2(SCN11A):c.-7-389A>G rs150766376 0.00466
NM_001349253.2(SCN11A):c.1474-207A>G rs141742044 0.00466
NM_001349253.2(SCN11A):c.386+150G>A rs183953683 0.00466
NM_001349253.2(SCN11A):c.387-208G>T rs146423084 0.00466
NM_001349253.2(SCN11A):c.618-128G>A rs183505905 0.00466
NM_001349253.2(SCN11A):c.712+276A>G rs147807728 0.00465
NM_001349253.2(SCN11A):c.-155C>T rs76870831 0.00457
NM_001349253.2(SCN11A):c.1473+31A>G rs145418857 0.00418
NM_001349253.2(SCN11A):c.1473+147T>C rs149865639 0.00417
NM_001349253.2(SCN11A):c.3132C>G (p.Asn1044Lys) rs35693485 0.00382
NM_001349253.2(SCN11A):c.892+176T>C rs57068397 0.00379
NM_001349253.2(SCN11A):c.1473+12C>T rs115646260 0.00378
NM_001349253.2(SCN11A):c.3064+85A>G rs75639842 0.00359
NM_001349253.2(SCN11A):c.4328-250A>C rs80340831 0.00359
NM_001349253.2(SCN11A):c.2950-65C>T rs113427543 0.00331
NM_001349253.2(SCN11A):c.267+73G>A rs553482172 0.00309
NM_001349253.2(SCN11A):c.4057-265T>A rs185529676 0.00301
NM_001349253.2(SCN11A):c.2213C>T (p.Pro738Leu) rs140995438 0.00163
NM_001349253.2(SCN11A):c.5207G>T (p.Gly1736Val) rs143852849 0.00151
NM_001349253.2(SCN11A):c.1843-10C>A rs200533903 0.00049
NM_001349253.2(SCN11A):c.3473T>C (p.Leu1158Pro) rs141686175 0.00047
NM_001349253.2(SCN11A):c.268-3C>T rs200598776 0.00037
NM_001349253.2(SCN11A):c.2298C>T (p.Cys766=) rs202104116 0.00017
NM_001349253.2(SCN11A):c.2513G>A (p.Arg838Gln) rs149681198 0.00016
NM_001349253.2(SCN11A):c.1097A>G (p.Gln366Arg) rs112707835 0.00013
NM_001349253.2(SCN11A):c.2433C>G (p.Leu811=) rs377615513 0.00012
NM_001349253.2(SCN11A):c.4153G>A (p.Ala1385Thr) rs755650500 0.00012
NM_001349253.2(SCN11A):c.4282G>A (p.Gly1428Ser) rs201336927 0.00012
NM_001349253.2(SCN11A):c.5359A>G (p.Lys1787Glu) rs199522402 0.00012
NM_001349253.2(SCN11A):c.712C>T (p.Arg238Cys) rs146942592 0.00012
NM_001349253.2(SCN11A):c.1744G>A (p.Ala582Thr) rs141228634 0.00011
NM_001349253.2(SCN11A):c.408C>T (p.Ile136=) rs148425367 0.00010
NM_001349253.2(SCN11A):c.4309G>A (p.Val1437Met) rs149699837 0.00010
NM_001349253.2(SCN11A):c.2945G>A (p.Arg982Gln) rs562379429 0.00006
NM_001349253.2(SCN11A):c.7G>C (p.Asp3His) rs373639733 0.00006
NM_001349253.2(SCN11A):c.5124A>G (p.Glu1708=) rs534882975 0.00004
NM_001349253.2(SCN11A):c.19C>G (p.Pro7Ala) rs372831672 0.00002
NM_001349253.2(SCN11A):c.1300-18C>G rs199549308 0.00001
NM_001349253.2(SCN11A):c.1437T>C (p.Pro479=) rs767647177 0.00001
NM_001349253.2(SCN11A):c.1696G>A (p.Val566Ile) rs201421435 0.00001
NM_001349253.2(SCN11A):c.2340G>A (p.Ala780=) rs779486096 0.00001
NM_001349253.2(SCN11A):c.2776G>A (p.Val926Ile) rs759255427 0.00001
NM_001349253.2(SCN11A):c.4014A>G (p.Lys1338=) rs554136131 0.00001
NM_001349253.2(SCN11A):c.5071G>A (p.Ala1691Thr) rs754911340 0.00001
NM_001349253.2(SCN11A):c.2403+44C>A rs202072876
NM_001349253.2(SCN11A):c.267+15dup rs375995524
NM_001349253.2(SCN11A):c.267+19G>C rs776868746
NM_001349253.2(SCN11A):c.267+28_267+30dup rs749134287
NM_001349253.2(SCN11A):c.267+30G>C
NM_001349253.2(SCN11A):c.268-10dup rs552650164
NM_001349253.2(SCN11A):c.268-5T>G rs760661204
NM_001349253.2(SCN11A):c.3065-261C>A rs140094178
NM_001349253.2(SCN11A):c.3078C>T (p.Cys1026=) rs1478821824
NM_001349253.2(SCN11A):c.3144C>T (p.Thr1048=) rs1575242555
NM_001349253.2(SCN11A):c.3760-6T>C rs1296524863
NM_001349253.2(SCN11A):c.3952-47A>T rs77497897
NM_001349253.2(SCN11A):c.4464T>C (p.Phe1488=)
NM_001349253.2(SCN11A):c.617+301_617+302dup rs869220907

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