Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.38557232C>A | CA018099 | SCN5A | c.4295G>T (p.Gly1432Val) c.4298G>T (p.Gly1433Val) c.4246-654G>T (n.4246-654G>T) c.4136G>T (p.Gly1379Val) c.4169G>T (p.Gly1390Val) c.4243-654G>T (n.4243-654G>T) | ClinVar dbSNP |
3 | g.38557232C>T | CA72943604 | SCN5A | c.4295G>A (p.Gly1432Glu) c.4298G>A (p.Gly1433Glu) c.4246-654G>A (n.4246-654G>A) c.4136G>A (p.Gly1379Glu) c.4169G>A (p.Gly1390Glu) c.4243-654G>A (n.4243-654G>A) | dbSNP |