ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as likely benign for not provided

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Total variants: 62
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HGVS dbSNP
NM_001365536.1(SCN9A):c.1110G>A (p.Thr370=) rs202002028
NM_001365536.1(SCN9A):c.1113G>A (p.Leu371=) rs1260914439
NM_001365536.1(SCN9A):c.1344A>G (p.Thr448=) rs747552653
NM_001365536.1(SCN9A):c.1398C>T (p.Ser466=) rs201531206
NM_001365536.1(SCN9A):c.1443G>A (p.Lys481=) rs1574868048
NM_001365536.1(SCN9A):c.1464C>T (p.Leu488=) rs200682458
NM_001365536.1(SCN9A):c.1695A>G (p.Gly565=) rs1574864584
NM_001365536.1(SCN9A):c.1713C>T (p.Ala571=) rs200876333
NM_001365536.1(SCN9A):c.1818T>C (p.Ser606=) rs202141567
NM_001365536.1(SCN9A):c.2055C>T (p.Leu685=) rs202048023
NM_001365536.1(SCN9A):c.2130T>C (p.Cys710=) rs1358344300
NM_001365536.1(SCN9A):c.2133A>C (p.Pro711=) rs1574857355
NM_001365536.1(SCN9A):c.2165T>C (p.Leu722Ser) rs187526567
NM_001365536.1(SCN9A):c.2190G>C (p.Trp730Cys) rs202055175
NM_001365536.1(SCN9A):c.2248A>G (p.Ile750Val) rs182650126
NM_001365536.1(SCN9A):c.2352T>C (p.Thr784=) rs1574853796
NM_001365536.1(SCN9A):c.2392A>G (p.Met798Val) rs149707354
NM_001365536.1(SCN9A):c.2475A>G (p.Leu825=) rs1574853488
NM_001365536.1(SCN9A):c.2595T>A (p.Ala865=) rs1574851833
NM_001365536.1(SCN9A):c.2691C>T (p.Cys897=) rs1060504427
NM_001365536.1(SCN9A):c.2964C>T (p.Leu988=) rs201430964
NM_001365536.1(SCN9A):c.2994A>C (p.Gly998=) rs1574844351
NM_001365536.1(SCN9A):c.3003T>C (p.Tyr1001=) rs886038521
NM_001365536.1(SCN9A):c.3141C>T (p.Ser1047=) rs1046258167
NM_001365536.1(SCN9A):c.3361C>T (p.Arg1121Trp) rs190664764
NM_001365536.1(SCN9A):c.3472+7C>A rs1458073270
NM_001365536.1(SCN9A):c.3612C>T (p.Leu1204=) rs1408476498
NM_001365536.1(SCN9A):c.3767A>G (p.Asn1256Ser) rs141268327
NM_001365536.1(SCN9A):c.3781C>T (p.Leu1261=) rs1574780648
NM_001365536.1(SCN9A):c.3832C>G (p.Leu1278Val) rs180922748
NM_001365536.1(SCN9A):c.4077T>C (p.Phe1359=) rs1205678504
NM_001365536.1(SCN9A):c.4227G>A (p.Thr1409=) rs970261148
NM_001365536.1(SCN9A):c.4315G>A (p.Val1439Ile) rs149346064
NM_001365536.1(SCN9A):c.4398+7A>G rs1574756110
NM_001365536.1(SCN9A):c.4399-6C>A rs1553474406
NM_001365536.1(SCN9A):c.4479A>T (p.Pro1493=) rs1223830877
NM_001365536.1(SCN9A):c.4503+9del rs759871579
NM_001365536.1(SCN9A):c.4545A>G (p.Gln1515=) rs1298398772
NM_001365536.1(SCN9A):c.4614T>C (p.Gly1538=) rs1250627204
NM_001365536.1(SCN9A):c.4645T>C (p.Trp1549Arg) rs202084411
NM_001365536.1(SCN9A):c.4677T>C (p.Thr1559=) rs773380999
NM_001365536.1(SCN9A):c.4686T>C (p.Cys1562=) rs201655242
NM_001365536.1(SCN9A):c.4767C>T (p.Ser1589=) rs200690956
NM_001365536.1(SCN9A):c.4794G>A (p.Leu1598=) rs1574694057
NM_001365536.1(SCN9A):c.4848G>A (p.Arg1616=) rs1574693824
NM_001365536.1(SCN9A):c.4923T>C (p.Leu1641=) rs199550149
NM_001365536.1(SCN9A):c.4941C>T (p.Ile1647=) rs747837371
NM_001365536.1(SCN9A):c.4953C>G (p.Leu1651=) rs776545037
NM_001365536.1(SCN9A):c.4959G>T (p.Leu1653=) rs768193278
NM_001365536.1(SCN9A):c.4974C>T (p.Tyr1658=) rs757858235
NM_001365536.1(SCN9A):c.5220T>C (p.Phe1740=) rs200817449
NM_001365536.1(SCN9A):c.5487C>A (p.Pro1829=) rs751325279
NM_001365536.1(SCN9A):c.5493T>G (p.Val1831=) rs1261742033
NM_001365536.1(SCN9A):c.5586G>A (p.Gln1862=) rs199572382
NM_001365536.1(SCN9A):c.5649A>G (p.Thr1883=) rs1574691120
NM_001365536.1(SCN9A):c.5697T>C (p.Ala1899=) rs1338674674
NM_001365536.1(SCN9A):c.5711G>A (p.Arg1904His) rs79805025
NM_001365536.1(SCN9A):c.5779C>T (p.Leu1927Phe) rs111558968
NM_001365536.1(SCN9A):c.5883A>G (p.Val1961=) rs1574690144
NM_001365536.1(SCN9A):c.927C>A (p.Ser309=) rs762274623
NM_001365536.1(SCN9A):c.957A>G (p.Thr319=) rs1574885699
NM_001365536.1(SCN9A):c.965+10A>G rs202185010

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