ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 74
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HGVS dbSNP gnomAD frequency
NM_001365536.1(SCN9A):c.3767A>G (p.Asn1256Ser) rs141268327 0.00496
NM_001365536.1(SCN9A):c.1398C>T (p.Ser466=) rs201531206 0.00386
NM_001365536.1(SCN9A):c.5779C>T (p.Leu1927Phe) rs111558968 0.00315
NM_001365536.1(SCN9A):c.3361C>T (p.Arg1121Trp) rs190664764 0.00304
NM_001365536.1(SCN9A):c.2248A>G (p.Ile750Val) rs182650126 0.00278
NM_001365536.1(SCN9A):c.4356C>T (p.Phe1452=) rs201145311 0.00263
NM_001365536.1(SCN9A):c.3506A>C (p.Asn1169Thr) rs151241025 0.00216
NM_001365536.1(SCN9A):c.1997A>G (p.Lys666Arg) rs121908919 0.00180
NM_001365536.1(SCN9A):c.3832C>G (p.Leu1278Val) rs180922748 0.00174
NM_001365536.1(SCN9A):c.4645T>C (p.Trp1549Arg) rs202084411 0.00173
NM_001365536.1(SCN9A):c.4314C>T (p.Val1438=) rs188336294 0.00171
NM_001365536.1(SCN9A):c.1326G>A (p.Ala442=) rs200065104 0.00102
NM_001365536.1(SCN9A):c.3329C>T (p.Ser1110Leu) rs145258166 0.00066
NM_001365536.1(SCN9A):c.4315G>A (p.Val1439Ile) rs149346064 0.00061
NM_001365536.1(SCN9A):c.1464C>T (p.Leu488=) rs200682458 0.00059
NM_001365536.1(SCN9A):c.1555G>A (p.Glu519Lys) rs187453572 0.00059
NM_001365536.1(SCN9A):c.3002A>G (p.Tyr1001Cys) rs199692186 0.00056
NM_001365536.1(SCN9A):c.3402G>T (p.Leu1134Phe) rs200160858 0.00052
NM_001365536.1(SCN9A):c.4923T>C (p.Leu1641=) rs199550149 0.00041
NM_001365536.1(SCN9A):c.2964C>T (p.Leu988=) rs201430964 0.00032
NM_001365536.1(SCN9A):c.4110T>C (p.Cys1370=) rs199673396 0.00019
NM_001365536.1(SCN9A):c.1099T>C (p.Tyr367His) rs200457046 0.00011
NM_001365536.1(SCN9A):c.1554C>T (p.Val518=) rs201054032 0.00009
NM_001365536.1(SCN9A):c.2085A>G (p.Ile695Met) rs199588089 0.00009
NM_001365536.1(SCN9A):c.4305T>G (p.Ile1435Met) rs200479892 0.00009
NM_001365536.1(SCN9A):c.1793G>A (p.Arg598His) rs201318927 0.00004
NM_001365536.1(SCN9A):c.4100G>A (p.Arg1367His) rs200566017 0.00004
NM_001365536.1(SCN9A):c.2437A>G (p.Ser813Gly) rs201890240 0.00003
NM_001365536.1(SCN9A):c.4156A>C (p.Lys1386Gln) rs199902747 0.00003
NM_001365536.1(SCN9A):c.4289G>A (p.Ser1430Asn) rs201479177 0.00003
NM_001365536.1(SCN9A):c.2166G>C (p.Leu722Phe) rs772492538 0.00002
NM_001365536.1(SCN9A):c.1108-5C>T rs201496520 0.00001
NM_001365536.1(SCN9A):c.1642C>T (p.Arg548Ter) rs1057518900 0.00001
NM_001365536.1(SCN9A):c.1792C>T (p.Arg598Cys) rs200065703 0.00001
NM_001365536.1(SCN9A):c.2052C>T (p.Asn684=) rs199668507 0.00001
NM_001365536.1(SCN9A):c.2191A>G (p.Ile731Val) rs1574857096 0.00001
NM_001365536.1(SCN9A):c.2330C>T (p.Ala777Val) rs749482425 0.00001
NM_001365536.1(SCN9A):c.2332A>G (p.Ile778Val) rs544352696 0.00001
NM_001365536.1(SCN9A):c.2712G>A (p.Thr904=) rs200494981 0.00001
NM_001365536.1(SCN9A):c.2779G>A (p.Glu927Lys) rs202097398 0.00001
NM_001365536.1(SCN9A):c.4077T>C (p.Phe1359=) rs1205678504 0.00001
NM_001365536.1(SCN9A):c.4668C>A (p.Ile1556=) rs771245206 0.00001
NM_001365536.1(SCN9A):c.4994A>G (p.Asn1665Ser) rs1401418949 0.00001
NM_001365536.1(SCN9A):c.5245C>T (p.Leu1749=) rs200636760 0.00001
NM_001365536.1(SCN9A):c.1113G>A (p.Leu371=) rs1260914439
NM_001365536.1(SCN9A):c.1198G>A (p.Val400Met) rs1553491169
NM_001365536.1(SCN9A):c.1286_1287delinsAA (p.Arg429Gln) rs1064797268
NM_001365536.1(SCN9A):c.1336G>A (p.Glu446Lys) rs1175228324
NM_001365536.1(SCN9A):c.1502C>T (p.Ser501Leu)
NM_001365536.1(SCN9A):c.1757G>A (p.Gly586Asp) rs1574864414
NM_001365536.1(SCN9A):c.2146A>C (p.Arg716=) rs1177414657
NM_001365536.1(SCN9A):c.2387T>C (p.Ile796Thr) rs2106471480
NM_001365536.1(SCN9A):c.2538A>G (p.Ala846=) rs922811520
NM_001365536.1(SCN9A):c.2576T>C (p.Ile859Thr) rs80356474
NM_001365536.1(SCN9A):c.3014C>A (p.Thr1005Asn) rs200155076
NM_001365536.1(SCN9A):c.3223G>A (p.Asp1075Asn)
NM_001365536.1(SCN9A):c.3289G>A (p.Asp1097Asn) rs768654039
NM_001365536.1(SCN9A):c.3622G>A (p.Ala1208Thr)
NM_001365536.1(SCN9A):c.3627+8A>T rs1553482000
NM_001365536.1(SCN9A):c.3928G>T (p.Val1310Phe) rs121908913
NM_001365536.1(SCN9A):c.4073G>A (p.Arg1358Gln) rs200163716
NM_001365536.1(SCN9A):c.4211C>A (p.Thr1404Asn) rs201880500
NM_001365536.1(SCN9A):c.4260+3A>G
NM_001365536.1(SCN9A):c.4343C>T (p.Thr1448Ile)
NM_001365536.1(SCN9A):c.4370T>C (p.Ile1457Thr) rs1694849428
NM_001365536.1(SCN9A):c.4480C>G (p.Gln1494Glu) rs201750475
NM_001365536.1(SCN9A):c.4533A>G (p.Leu1511=) rs545627123
NM_001365536.1(SCN9A):c.4597A>T (p.Met1533Leu) rs2106346393
NM_001365536.1(SCN9A):c.4698G>T (p.Leu1566=)
NM_001365536.1(SCN9A):c.5212T>G (p.Phe1738Val) rs763972874
NM_001365536.1(SCN9A):c.5254G>C (p.Val1752Leu) rs1064797267
NM_001365536.1(SCN9A):c.5336T>A (p.Phe1779Tyr)
NM_001365536.1(SCN9A):c.5371C>A (p.Pro1791Thr) rs1693360658
NM_001365536.1(SCN9A):c.981G>C (p.Gly327=)

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