ClinVar Miner

List of variants in gene SCN10A reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_006514.4(SCN10A):c.45C>T (p.Arg15=) rs34314583 0.00684
NM_006514.4(SCN10A):c.4009T>A (p.Ser1337Thr) rs11711062 0.00451
NM_006514.4(SCN10A):c.4416C>T (p.Ile1472=) rs144944369 0.00267
NM_006514.4(SCN10A):c.4568G>A (p.Cys1523Tyr) rs142217269 0.00134
NM_006514.4(SCN10A):c.-8A>T rs200901459 0.00123
NM_006514.4(SCN10A):c.3674T>C (p.Ile1225Thr) rs139638446 0.00048
NM_006514.4(SCN10A):c.969T>C (p.Tyr323=) rs143668889 0.00023
NM_006514.4(SCN10A):c.694C>T (p.Leu232=) rs200583405 0.00011
NM_006514.4(SCN10A):c.5370G>T (p.Leu1790=) rs140566252 0.00009
NM_006514.4(SCN10A):c.3705G>A (p.Ala1235=) rs147376215 0.00006
NM_006514.4(SCN10A):c.4660C>T (p.Leu1554=) rs745999522 0.00006
NM_006514.4(SCN10A):c.1890G>A (p.Lys630=) rs764191883 0.00005
NM_006514.4(SCN10A):c.4917C>T (p.Asp1639=) rs142804903 0.00004
NM_006514.4(SCN10A):c.2208C>T (p.Ile736=) rs754351607 0.00001
NM_006514.4(SCN10A):c.630G>A (p.Gly210=) rs750830318 0.00001
NM_006514.4(SCN10A):c.2313C>T (p.Pro771=)
NM_006514.4(SCN10A):c.5476GAG[1] (p.Glu1827del) rs772082757
NM_006514.4(SCN10A):c.5587C>A (p.Arg1863=)

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