Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.38575385C>T | CA017287 | SCN5A | c.3575G>A (p.Arg1192Gln) c.3578G>A (p.Arg1193Gln) c.3416G>A (p.Arg1139Gln) c.3449G>A (p.Arg1150Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.38575385C= | CA1358572562 | SCN5A | c.3575G= (p.Arg1192=) c.3578G= (p.Arg1193=) c.3416G= (p.Arg1139=) c.3449G= (p.Arg1150=) | dbSNP |