Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.5225705A>C | CA379273734 | HBB | c.337T>G (p.Cys113Gly) n.269T>G c.*153T>G (n.*153T>G) | dbSNP |
11 | g.5225705A>G | CA124924 | HBB | c.337T>C (p.Cys113Arg) n.269T>C c.*153T>C (n.*153T>C) | ClinVar dbSNP |
11 | g.5225705A= | CA1949565122 | HBB | c.337T= (p.Cys113=) n.269T= c.*153T= (n.*153T=) | dbSNP |