ClinVar Miner

List of variants in gene combination LOC110121288, SCN10A reported as likely benign for Brugada syndrome

Included ClinVar conditions (45):
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Gene type:
ClinVar version:
Total variants: 62
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HGVS dbSNP gnomAD frequency
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.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.2973G>A (p.Pro991=) rs201397469 0.00006
NM_006514.4(SCN10A):c.2988T>C (p.Ser996=) rs375913659 0.00006
NM_006514.4(SCN10A):c.3156A>G (p.Thr1052=) rs777642089 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.3138G>A (p.Arg1046=) rs371613636 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.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.2994C>T (p.Pro998=) rs200267333 0.00002
NM_006514.4(SCN10A):c.2817C>T (p.Pro939=) rs374319726 0.00001
NM_006514.4(SCN10A):c.3087+7G>A rs761835406 0.00001
NM_006514.4(SCN10A):c.3180C>T (p.Ser1060=) rs1209864756 0.00001
NM_006514.4(SCN10A):c.3243A>G (p.Thr1081=) rs749507043 0.00001
NM_006514.4(SCN10A):c.3507+10G>A rs767411176 0.00001
NM_006514.4(SCN10A):c.2796C>T (p.Phe932=) rs2126001483
NM_006514.4(SCN10A):c.2826G>A (p.Lys942=)
NM_006514.4(SCN10A):c.2832G>A (p.Glu944=)
NM_006514.4(SCN10A):c.2841G>T (p.Leu947=) rs765937462
NM_006514.4(SCN10A):c.2901C>A (p.Ala967=)
NM_006514.4(SCN10A):c.2902A>C (p.Arg968=) rs746193804
NM_006514.4(SCN10A):c.2910C>T (p.Ser970=)
NM_006514.4(SCN10A):c.2922C>T (p.Leu974=)
NM_006514.4(SCN10A):c.2940C>G (p.Pro980=) rs1192005964
NM_006514.4(SCN10A):c.2949G>A (p.Glu983=)
NM_006514.4(SCN10A):c.2976T>C (p.Thr992=)
NM_006514.4(SCN10A):c.3009A>G (p.Glu1003=)
NM_006514.4(SCN10A):c.3087+18G>A
NM_006514.4(SCN10A):c.3087+20G>T
NM_006514.4(SCN10A):c.3088-13C>A
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.3108C>T (p.Val1036=) rs970173552
NM_006514.4(SCN10A):c.3112A>C (p.Arg1038=)
NM_006514.4(SCN10A):c.3114G>A (p.Arg1038=)
NM_006514.4(SCN10A):c.3174T>C (p.Ala1058=)
NM_006514.4(SCN10A):c.3181C>T (p.Leu1061=)
NM_006514.4(SCN10A):c.3229-11C>T
NM_006514.4(SCN10A):c.3231A>C (p.Gly1077=)
NM_006514.4(SCN10A):c.3255G>A (p.Glu1085=) rs143610297
NM_006514.4(SCN10A):c.3318T>C (p.Asp1106=)
NM_006514.4(SCN10A):c.3352+20C>T
NM_006514.4(SCN10A):c.3353-14A>C
NM_006514.4(SCN10A):c.3353-4A>G rs2125997358
NM_006514.4(SCN10A):c.3361C>A (p.Arg1121Ser) rs146965005
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.3495C>T (p.Ser1165=)
NM_006514.4(SCN10A):c.3507+13A>C
NM_006514.4(SCN10A):c.3507+13A>G
NM_006514.4(SCN10A):c.3507+16G>C
NM_006514.4(SCN10A):c.3507+8G>A

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