Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.38551504C>T | CA018670 | SCN5A | c.4865G>A (p.Arg1622Gln) c.4868G>A (p.Arg1623Gln) c.4814G>A (p.Arg1605Gln) c.4706G>A (p.Arg1569Gln) c.4769G>A (p.Arg1590Gln) c.4739G>A (p.Arg1580Gln) c.4811G>A (p.Arg1604Gln) | ClinVar dbSNP |
3 | g.38551504C>A | CA018677 | SCN5A | c.4865G>T (p.Arg1622Leu) c.4868G>T (p.Arg1623Leu) c.4814G>T (p.Arg1605Leu) c.4706G>T (p.Arg1569Leu) c.4769G>T (p.Arg1590Leu) c.4739G>T (p.Arg1580Leu) c.4811G>T (p.Arg1604Leu) | ClinVar dbSNP |