Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.5226621C>T | CA124716 | HBB | c.271G>A (p.Glu91Lys) c.271G>A n.203G>A n.322G>A c.*87G>A (n.*87G>A) | ClinVar dbSNP gnomAD v4 |
11 | g.5226621C>A | CA125368 | HBB | c.271G>T (p.Glu91Ter) c.271G>T n.203G>T n.322G>T c.*87G>T (n.*87G>T) | ClinVar dbSNP |
11 | g.5226621C= | CA1949567718 | HBB | c.271G= (p.Glu91=) c.271G= n.203G= n.322G= c.*87G= (n.*87G=) | dbSNP |