Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.41978041G>A | CA341233 | ATP1A3 | c.1877C>T (p.Thr626Met) c.1838C>T (p.Thr613Met) c.1871C>T (p.Thr624Met) c.1748C>T (p.Thr583Met) | ClinVar dbSNP COSMIC |
19 | g.41978041G= | CA2336724849 | ATP1A3 | c.1877C= (p.Thr626=) c.1838C= (p.Thr613=) c.1871C= (p.Thr624=) c.1748C= (p.Thr583=) | dbSNP |