ClinVar Miner

List of variants in gene combination LOC110121288, SCN10A studied for not provided

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Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_006514.4(SCN10A):c.3352+139C>A rs4076737 0.69339
NM_006514.4(SCN10A):c.3088-510A>G rs6801957 0.67159
NM_006514.4(SCN10A):c.3228+317A>G rs62242438 0.22203
NM_006514.4(SCN10A):c.3353-168G>A rs61487238 0.21698
NM_006514.4(SCN10A):c.3352+263C>A rs59733668 0.07567
NM_006514.4(SCN10A):c.3352+136G>A rs77019133 0.03755
NM_006514.4(SCN10A):c.3087+41G>A rs77787358 0.01345
NM_006514.4(SCN10A):c.3229-124C>T rs75660637 0.01336
NM_006514.4(SCN10A):c.3353-275G>A rs74348091 0.01334
NM_006514.4(SCN10A):c.3352+287A>G rs77304538 0.01184
NM_006514.4(SCN10A):c.3088-276A>G rs76534052 0.01016
NM_006514.4(SCN10A):c.3087+15C>T rs140924179 0.00650
NM_006514.4(SCN10A):c.3088-218A>C rs79868348 0.00475
NM_006514.4(SCN10A):c.3352+222G>A rs75276273 0.00377
NM_006514.4(SCN10A):c.3229-178C>T rs147354941 0.00294
NM_006514.4(SCN10A):c.3353-63G>C rs188832627 0.00279
NM_006514.4(SCN10A):c.3229-20C>T rs73825880 0.00248
NM_006514.4(SCN10A):c.3507+38G>T rs181688711 0.00089
NM_006514.4(SCN10A):c.2972C>T (p.Pro991Leu) rs138413438 0.00068
NM_006514.4(SCN10A):c.2842G>C (p.Val948Leu) rs145694222 0.00044
NM_006514.4(SCN10A):c.3482T>C (p.Met1161Thr) rs200713724 0.00029
NM_006514.4(SCN10A):c.2816C>T (p.Pro939Leu) rs202174472 0.00013
NM_006514.4(SCN10A):c.3417G>C (p.Trp1139Cys) rs143744796 0.00013
NM_006514.4(SCN10A):c.2814C>T (p.Phe938=) rs200870389 0.00011
NM_006514.4(SCN10A):c.3445G>A (p.Val1149Met) rs560631745 0.00009
NM_006514.4(SCN10A):c.3238G>A (p.Asp1080Asn) rs376528831 0.00008
NM_006514.4(SCN10A):c.3340T>C (p.Cys1114Arg) rs771127702 0.00007
NM_006514.4(SCN10A):c.2973G>A (p.Pro991=) rs201397469 0.00006
NM_006514.4(SCN10A):c.3010T>G (p.Ser1004Ala) rs186031413 0.00006
NM_006514.4(SCN10A):c.3425G>A (p.Arg1142His) rs200584416 0.00006
NM_006514.4(SCN10A):c.3439C>T (p.Arg1147Cys) rs373470651 0.00006
NM_006514.4(SCN10A):c.3156A>G (p.Thr1052=) rs777642089 0.00004
NM_006514.4(SCN10A):c.3178T>G (p.Ser1060Ala) rs750655728 0.00004
NM_006514.4(SCN10A):c.3354A>G (p.Gly1118=) rs770004970 0.00004
NM_006514.4(SCN10A):c.2809C>T (p.Pro937Ser) rs1029017064 0.00003
NM_006514.4(SCN10A):c.3138G>A (p.Arg1046=) rs371613636 0.00003
NM_006514.4(SCN10A):c.2994C>T (p.Pro998=) rs200267333 0.00002
NM_006514.4(SCN10A):c.3070G>A (p.Val1024Met) rs201106879 0.00002
NM_006514.4(SCN10A):c.3474C>G (p.Ile1158Met) rs145568435 0.00002
NM_006514.4(SCN10A):c.2852T>A (p.Leu951His) rs755728923 0.00001
NM_006514.4(SCN10A):c.2906G>A (p.Gly969Glu) rs2063460316 0.00001
NM_006514.4(SCN10A):c.2979G>A (p.Val993=) rs1052388906 0.00001
NM_006514.4(SCN10A):c.3229-1G>A rs1408879863 0.00001
NM_006514.4(SCN10A):c.3374G>C (p.Cys1125Ser) rs1481868189 0.00001
NM_006514.4(SCN10A):c.3475A>G (p.Ile1159Val) rs753434251 0.00001
NM_006514.4(SCN10A):c.2826G>A (p.Lys942=)
NM_006514.4(SCN10A):c.2853C>A (p.Leu951=) rs767245856
NM_006514.4(SCN10A):c.2955_3018delinsAGACCCATC (p.Ser985fs) rs2126001161
NM_006514.4(SCN10A):c.3020A>G (p.Asp1007Gly)
NM_006514.4(SCN10A):c.3087+136T>G rs59858965
NM_006514.4(SCN10A):c.3108C>T (p.Val1036=) rs970173552
NM_006514.4(SCN10A):c.3118_3130delinsCCAGGCACTGGAACATCTTCTGAG (p.Gly1040fs) rs2126000030
NM_006514.4(SCN10A):c.3131C>T (p.Thr1044Ile)
NM_006514.4(SCN10A):c.3355T>A (p.Cys1119Ser) rs1450059546
NM_006514.4(SCN10A):c.3361C>A (p.Arg1121Ser) rs146965005
NM_006514.4(SCN10A):c.3361C>T (p.Arg1121Cys) rs146965005
NM_006514.4(SCN10A):c.3486C>A (p.Ile1162=) rs1575954364

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