ClinVar Miner

List of variants in gene combination LOC110121288, SCN10A reported as uncertain significance by GeneDx

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Total variants: 23
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HGVS dbSNP gnomAD frequency
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.3445G>A (p.Val1149Met) rs560631745 0.00009
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.2809C>T (p.Pro937Ser) rs1029017064 0.00003
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.3374G>C (p.Cys1125Ser) rs1481868189 0.00001
NM_006514.4(SCN10A):c.3475A>G (p.Ile1159Val) rs753434251 0.00001
NM_006514.4(SCN10A):c.2955_3018delinsAGACCCATC (p.Ser985fs) rs2126001161
NM_006514.4(SCN10A):c.3020A>G (p.Asp1007Gly)
NM_006514.4(SCN10A):c.3108C>T (p.Val1036=) rs970173552
NM_006514.4(SCN10A):c.3131C>T (p.Thr1044Ile)
NM_006514.4(SCN10A):c.3304C>T (p.Pro1102Ser) rs1057518542
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

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