Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.5225669G>T | CA379273701 | HBB | c.373C>A (p.Pro125Thr) n.305C>A c.*189C>A (n.*189C>A) | ClinVar dbSNP |
11 | g.5225669G>A | CA125217 | HBB | c.373C>T (p.Pro125Ser) n.305C>T c.*189C>T (n.*189C>T) | ClinVar dbSNP |
11 | g.5225669G= | CA1949564819 | HBB | c.373C= (p.Pro125=) n.305C= c.*189C= (n.*189C=) | dbSNP |