Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.38609764C>T | CA352150375 | SCN5A | c.904G>A (p.Glu302Lys) c.775G>A (p.Glu259Lys) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
3 | g.38609764C>A | CA16611395 | SCN5A | c.904G>T (p.Glu302Ter) c.775G>T (p.Glu259Ter) | ClinVar dbSNP |
3 | g.38609764C= | CA1358587636 | SCN5A | c.904G= (p.Glu302=) c.775G= (p.Glu259=) | dbSNP |