Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.41985082C>T | CA341235 | ATP1A3 | c.868G>A (p.Glu290Lys) c.829G>A (p.Glu277Lys) c.739G>A (p.Glu247Lys) n.142G>A c.862G>A (p.Glu288Lys) | ClinVar dbSNP COSMIC |
19 | g.41985082C>G | CA406052917 | ATP1A3 | c.868G>C (p.Glu290Gln) c.829G>C (p.Glu277Gln) c.739G>C (p.Glu247Gln) n.142G>C c.862G>C (p.Glu288Gln) | dbSNP |
19 | g.41985082C= | CA2336728021 | ATP1A3 | c.868G= (p.Glu290=) c.829G= (p.Glu277=) c.739G= (p.Glu247=) n.142G= c.862G= (p.Glu288=) | dbSNP |