ClinVar Miner

List of variants in gene SCN5A reported as benign by Color

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Total variants: 36
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HGVS dbSNP
NM_000335.4(SCN5A):c.100C>T (p.Arg34Cys) rs6791924
NM_000335.4(SCN5A):c.1017C>T (p.Tyr339=) rs17215493
NM_000335.4(SCN5A):c.1068T>C (p.Asp356=) rs41313703
NM_000335.4(SCN5A):c.1141-3C>A rs41312433
NM_000335.4(SCN5A):c.1302C>T (p.Phe434=) rs41313699
NM_000335.4(SCN5A):c.1381T>G (p.Leu461Val) rs41313697
NM_000335.4(SCN5A):c.1441C>T (p.Arg481Trp) rs144511230
NM_000335.4(SCN5A):c.1569T>A (p.Arg523=) rs41313693
NM_000335.4(SCN5A):c.1571C>A (p.Ser524Tyr) rs41313691
NM_000335.4(SCN5A):c.1587T>C (p.Ile529=) rs45624133
NM_000335.4(SCN5A):c.1673A>G (p.His558Arg) rs1805124
NM_000335.4(SCN5A):c.1681C>T (p.Leu561=) rs45522138
NM_000335.4(SCN5A):c.1715C>A (p.Ala572Asp) rs36210423
NM_000335.4(SCN5A):c.1743G>A (p.Ser581=) rs41313687
NM_000335.4(SCN5A):c.1852C>T (p.Leu618Phe) rs45488304
NM_000335.4(SCN5A):c.2014G>A (p.Ala672Thr) rs199473140
NM_000335.4(SCN5A):c.354C>T (p.His118=) rs45533640
NM_000335.4(SCN5A):c.3575G>A (p.Arg1192Gln) rs41261344
NM_000335.4(SCN5A):c.3870G>A (p.Leu1290=) rs41313033
NM_000335.4(SCN5A):c.4215G>A (p.Gly1405=) rs41311123
NM_000335.4(SCN5A):c.4297-14T>C rs56104887
NM_000335.4(SCN5A):c.4299T>C (p.Tyr1433=) rs200556220
NM_000335.4(SCN5A):c.4821C>T (p.Leu1607=) rs45437099
NM_000335.4(SCN5A):c.4845C>T (p.Phe1615=) rs41315495
NM_000335.4(SCN5A):c.486C>T (p.Tyr162=) rs45489099
NM_000335.4(SCN5A):c.5357G>A (p.Ser1786Asn) rs199473316
NM_000335.4(SCN5A):c.5454T>C (p.Asp1818=) rs1805126
NM_000335.4(SCN5A):c.5604C>T (p.Asp1868=) rs560476223
NM_000335.4(SCN5A):c.5709G>A (p.Ser1903=) rs376826051
NM_000335.4(SCN5A):c.5793G>A (p.Ala1931=) rs200594132
NM_000335.4(SCN5A):c.5841C>T (p.Ile1947=) rs13324293
NM_000335.4(SCN5A):c.5848G>T (p.Val1950Leu) rs41315493
NM_000335.4(SCN5A):c.6000C>T (p.Leu2000=) rs538707712
NM_000335.4(SCN5A):c.717C>T (p.Ile239=) rs41285129
NM_000335.4(SCN5A):c.795C>T (p.Ala265=) rs527692731
NM_000335.4(SCN5A):c.87A>G (p.Ala29=) rs6599230

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