ClinVar Miner

List of variants in gene LOC110121288, SCN10A studied for Brugada syndrome

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Total variants: 148
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HGVS dbSNP gnomAD frequency
NM_006514.4(SCN10A):c.3218T>C (p.Val1073Ala) rs6795970 0.70355
NM_006514.4(SCN10A):c.3088-510A>G rs6801957 0.67159
NM_006514.4(SCN10A):c.3275T>C (p.Leu1092Pro) rs12632942 0.21722
NM_006514.4(SCN10A):c.3393C>G (p.Thr1131=) rs6771157 0.21708
NM_006514.4(SCN10A):c.2884A>G (p.Ile962Val) rs57326399 0.20797
NM_006514.4(SCN10A):c.2937C>T (p.Gly979=) rs59468016 0.18899
NM_006514.4(SCN10A):c.3192G>A (p.Thr1064=) rs6791171 0.15667
NM_006514.4(SCN10A):c.3088-20T>C rs11129804 0.06869
NM_006514.4(SCN10A):c.3133C>A (p.Pro1045Thr) rs73062575 0.01804
NM_006514.4(SCN10A):c.3087+15C>T rs140924179 0.00650
NM_006514.4(SCN10A):c.3229-20C>T rs73825880 0.00248
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.3291C>G (p.Ile1097Met) rs148041371 0.00031
NM_006514.4(SCN10A):c.3482T>C (p.Met1161Thr) rs200713724 0.00029
NM_006514.4(SCN10A):c.3152G>A (p.Gly1051Glu) rs528738403 0.00022
NM_006514.4(SCN10A):c.3173C>T (p.Ala1058Val) rs370202955 0.00018
NM_006514.4(SCN10A):c.2874T>C (p.Ala958=) rs776705318 0.00015
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.2988T>C (p.Ser996=) rs375913659 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.2936G>T (p.Gly979Val) rs559166014 0.00005
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.3234G>A (p.Val1078=) rs889915256 0.00004
NM_006514.4(SCN10A):c.3354A>G (p.Gly1118=) rs770004970 0.00004
NM_006514.4(SCN10A):c.3061C>T (p.Gln1021Ter) rs751252167 0.00003
NM_006514.4(SCN10A):c.3138G>A (p.Arg1046=) rs371613636 0.00003
NM_006514.4(SCN10A):c.3151G>A (p.Gly1051Arg) rs374447261 0.00003
NM_006514.4(SCN10A):c.3237C>T (p.Asp1079=) rs745921364 0.00003
NM_006514.4(SCN10A):c.3264G>A (p.Thr1088=) rs139332101 0.00003
NM_006514.4(SCN10A):c.3394A>C (p.Lys1132Gln) rs756848600 0.00003
NM_006514.4(SCN10A):c.3440G>A (p.Arg1147His) rs375926577 0.00003
NM_006514.4(SCN10A):c.2844G>A (p.Val948=) rs1364529882 0.00002
NM_006514.4(SCN10A):c.2922C>G (p.Leu974=) rs778416357 0.00002
NM_006514.4(SCN10A):c.2974A>G (p.Thr992Ala) rs765269419 0.00002
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.3157T>A (p.Ser1053Thr) rs962402134 0.00002
NM_006514.4(SCN10A):c.3191C>T (p.Thr1064Met) rs774803610 0.00002
NM_006514.4(SCN10A):c.3403T>C (p.Trp1135Arg) rs769714725 0.00002
NM_006514.4(SCN10A):c.3474C>G (p.Ile1158Met) rs145568435 0.00002
NM_006514.4(SCN10A):c.2817C>T (p.Pro939=) rs374319726 0.00001
NM_006514.4(SCN10A):c.2833C>T (p.Pro945Ser) rs372907454 0.00001
NM_006514.4(SCN10A):c.2852T>A (p.Leu951His) rs755728923 0.00001
NM_006514.4(SCN10A):c.2923C>T (p.Gln975Ter) rs755553717 0.00001
NM_006514.4(SCN10A):c.2935G>T (p.Gly979Cys) rs752287839 0.00001
NM_006514.4(SCN10A):c.2939C>T (p.Pro980Leu) rs751340142 0.00001
NM_006514.4(SCN10A):c.2965G>A (p.Ala989Thr) rs766280701 0.00001
NM_006514.4(SCN10A):c.2993C>T (p.Pro998Leu) rs775672433 0.00001
NM_006514.4(SCN10A):c.3000T>A (p.Ala1000=) rs778351672 0.00001
NM_006514.4(SCN10A):c.3087+2T>C rs765046340 0.00001
NM_006514.4(SCN10A):c.3087+7G>A rs761835406 0.00001
NM_006514.4(SCN10A):c.3114G>T (p.Arg1038Ser) rs773394234 0.00001
NM_006514.4(SCN10A):c.3130A>G (p.Thr1044Ala) rs147093541 0.00001
NM_006514.4(SCN10A):c.3180C>T (p.Ser1060=) rs1209864756 0.00001
NM_006514.4(SCN10A):c.3214C>T (p.Gln1072Ter) rs1458693100 0.00001
NM_006514.4(SCN10A):c.3243A>G (p.Thr1081=) rs749507043 0.00001
NM_006514.4(SCN10A):c.3280C>A (p.Pro1094Thr) rs973127854 0.00001
NM_006514.4(SCN10A):c.3289A>C (p.Ile1097Leu) rs1397301108 0.00001
NM_006514.4(SCN10A):c.3328G>C (p.Glu1110Gln) rs201871493 0.00001
NM_006514.4(SCN10A):c.3374G>C (p.Cys1125Ser) rs1481868189 0.00001
NM_006514.4(SCN10A):c.3409G>A (p.Val1137Met) rs1278228854 0.00001
NM_006514.4(SCN10A):c.3421G>A (p.Val1141Met) rs112412281 0.00001
NM_006514.4(SCN10A):c.3476T>A (p.Ile1159Asn) rs777240104 0.00001
NM_006514.4(SCN10A):c.3479T>C (p.Phe1160Ser) rs2063398350 0.00001
NM_006514.4(SCN10A):c.3507+10G>A rs767411176 0.00001
NM_006514.4(SCN10A):c.2779G>T (p.Ala927Ser) rs774405519
NM_006514.4(SCN10A):c.2796C>T (p.Phe932=) rs2126001483
NM_006514.4(SCN10A):c.2818C>A (p.Gln940Lys)
NM_006514.4(SCN10A):c.2830G>A (p.Glu944Lys)
NM_006514.4(SCN10A):c.2832G>A (p.Glu944=)
NM_006514.4(SCN10A):c.2832G>T (p.Glu944Asp)
NM_006514.4(SCN10A):c.2841G>T (p.Leu947=) rs765937462
NM_006514.4(SCN10A):c.2842G>A (p.Val948Met) rs145694222
NM_006514.4(SCN10A):c.2850A>G (p.Lys950=) rs7374804
NM_006514.4(SCN10A):c.2850A>T (p.Lys950Asn) rs7374804
NM_006514.4(SCN10A):c.2854C>G (p.Pro952Ala) rs370880796
NM_006514.4(SCN10A):c.2855C>T (p.Pro952Leu) rs774315933
NM_006514.4(SCN10A):c.2863A>T (p.Ser955Cys) rs1674245596
NM_006514.4(SCN10A):c.2901C>A (p.Ala967=)
NM_006514.4(SCN10A):c.2902A>C (p.Arg968=) rs746193804
NM_006514.4(SCN10A):c.2902del (p.Arg968fs) rs1553616744
NM_006514.4(SCN10A):c.2910C>T (p.Ser970=)
NM_006514.4(SCN10A):c.2917G>A (p.Gly973Arg)
NM_006514.4(SCN10A):c.2922C>T (p.Leu974=)
NM_006514.4(SCN10A):c.2940C>G (p.Pro980=) rs1192005964
NM_006514.4(SCN10A):c.3002_3005del (p.Glu1001fs) rs2126001175
NM_006514.4(SCN10A):c.3009A>G (p.Glu1003=)
NM_006514.4(SCN10A):c.3016C>G (p.Leu1006Val) rs963394464
NM_006514.4(SCN10A):c.3038G>A (p.Gly1013Asp) rs1228092020
NM_006514.4(SCN10A):c.3056G>A (p.Ser1019Asn)
NM_006514.4(SCN10A):c.3077C>T (p.Pro1026Leu) rs2063457731
NM_006514.4(SCN10A):c.3087+20G>T
NM_006514.4(SCN10A):c.3088-14C>T
NM_006514.4(SCN10A):c.3088-180_3088-5del rs2126000100
NM_006514.4(SCN10A):c.3088-20T>G
NM_006514.4(SCN10A):c.3088-4C>G
NM_006514.4(SCN10A):c.3095del (p.Gln1032fs)
NM_006514.4(SCN10A):c.3098T>A (p.Leu1033Gln) rs751664345
NM_006514.4(SCN10A):c.3108C>T (p.Val1036=) rs970173552
NM_006514.4(SCN10A):c.3114G>A (p.Arg1038=)
NM_006514.4(SCN10A):c.3116G>A (p.Cys1039Tyr) rs765623505
NM_006514.4(SCN10A):c.3116G>T (p.Cys1039Phe)
NM_006514.4(SCN10A):c.3134C>G (p.Pro1045Arg) rs2126000012
NM_006514.4(SCN10A):c.3140G>A (p.Ser1047Asn)
NM_006514.4(SCN10A):c.3140G>C (p.Ser1047Thr) rs771555935
NM_006514.4(SCN10A):c.3170T>G (p.Leu1057Arg) rs1559424975
NM_006514.4(SCN10A):c.3174T>C (p.Ala1058=)
NM_006514.4(SCN10A):c.3176C>T (p.Pro1059Leu)
NM_006514.4(SCN10A):c.3181C>T (p.Leu1061=)
NM_006514.4(SCN10A):c.3201T>A (p.Asp1067Glu)
NM_006514.4(SCN10A):c.3228+11C>A
NM_006514.4(SCN10A):c.3228+6T>A rs748066260
NM_006514.4(SCN10A):c.3229-11C>T
NM_006514.4(SCN10A):c.3230G>A (p.Gly1077Glu) rs1309415508
NM_006514.4(SCN10A):c.3231A>C (p.Gly1077=)
NM_006514.4(SCN10A):c.3233T>C (p.Val1078Ala)
NM_006514.4(SCN10A):c.3237C>A (p.Asp1079Glu) rs745921364
NM_006514.4(SCN10A):c.3255G>A (p.Glu1085=) rs143610297
NM_006514.4(SCN10A):c.3256G>T (p.Gly1086Cys) rs755448967
NM_006514.4(SCN10A):c.3299A>G (p.Lys1100Arg) rs928529158
NM_006514.4(SCN10A):c.3318T>C (p.Asp1106=)
NM_006514.4(SCN10A):c.3347C>T (p.Thr1116Ile) rs778116360
NM_006514.4(SCN10A):c.3352+20C>T
NM_006514.4(SCN10A):c.3353-4A>G rs2125997358
NM_006514.4(SCN10A):c.3355T>A (p.Cys1119Ser) rs1450059546
NM_006514.4(SCN10A):c.3358A>C (p.Ile1120Leu)
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.3362G>A (p.Arg1121His)
NM_006514.4(SCN10A):c.3386A>C (p.Asp1129Ala) rs1274496159
NM_006514.4(SCN10A):c.3393C>T (p.Thr1131=)
NM_006514.4(SCN10A):c.3468C>T (p.Ser1156=) rs1348668186
NM_006514.4(SCN10A):c.3474C>T (p.Ile1158=)
NM_006514.4(SCN10A):c.3481A>G (p.Met1161Val)
NM_006514.4(SCN10A):c.3495C>T (p.Ser1165=)
NM_006514.4(SCN10A):c.3507+13A>C
NM_006514.4(SCN10A):c.3507+16G>C
NM_006514.4(SCN10A):c.3507+8G>A

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