Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.74200787G>A | CA249480 | ADK | c.89G>A (p.Gly30Glu) c.38G>A (p.Gly13Glu) c.-484G>A (n.-484G>A) n.336G>A c.5G>A (p.Gly2Glu) | ClinVar dbSNP |
10 | g.74200787G= | CA1919951447 | ADK | c.89G= (p.Gly30=) c.38G= (p.Gly13=) c.-484G= (n.-484G=) n.336G= c.5G= (p.Gly2=) | dbSNP |