Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.27463607A>T | CA341466 | CHRNA2 | c.836T>A (p.Ile279Asn) c.*666T>A (n.*666T>A) c.791T>A (p.Ile264Asn) n.290-1853T>A c.770T>A (p.Ile257Asn) c.*238T>A (n.*238T>A) c.359T>A (p.Ile120Asn) c.242T>A (p.Ile81Asn) | ClinVar dbSNP |
8 | g.27463607A= | CA1772814478 | CHRNA2 | c.836T= (p.Ile279=) c.*666T= (n.*666T=) c.791T= (p.Ile264=) n.290-1853T= c.770T= (p.Ile257=) c.*238T= (n.*238T=) c.359T= (p.Ile120=) c.242T= (p.Ile81=) | dbSNP |