Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.41986163C>T | CA10576143 | ATP1A3 | c.463G>A (p.Ala155Thr) c.424G>A (p.Ala142Thr) n.539G>A c.334G>A (p.Ala112Thr) c.457G>A (p.Ala153Thr) | dbSNP |
19 | g.41986163C>A | CA406055326 | ATP1A3 | c.463G>T (p.Ala155Ser) c.424G>T (p.Ala142Ser) n.539G>T c.334G>T (p.Ala112Ser) c.457G>T (p.Ala153Ser) | dbSNP gnomAD v4 |