Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.102208210G>A | CA117487 | RRM2B | c.979C>T (p.Arg327Ter) n.366C>T c.823C>T (p.Arg275Ter) c.343C>T (p.Arg115Ter) c.124C>T (p.Arg42Ter) c.1148C>T c.312C>T (n.312C>T) c.817C>T (p.Arg273Ter) c.1195C>T (p.Arg399Ter) | ClinVar dbSNP COSMIC |
8 | g.102208210G= | CA1806674678 | RRM2B | c.979C= (p.Arg327=) n.366C= c.823C= (p.Arg275=) c.343C= (p.Arg115=) c.124C= (p.Arg42=) c.1148C= c.312C= (n.312C=) c.817C= (p.Arg273=) c.1195C= (p.Arg399=) | dbSNP |