Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.67365138A>G | CA342144 | CLCF1,RAD9A | c.676T>C (p.Ter226Arg) c.646T>C (p.Ter216Arg) c.16+8386T>C (n.16+8386T>C) n.392-22397A>G n.424-22397A>G | ClinVar dbSNP |
11 | g.67365138A= | CA1980082155 | CLCF1,RAD9A | c.676T= (p.Ter226=) c.646T= (p.Ter216=) c.16+8386T= (n.16+8386T=) n.392-22397A= n.424-22397A= | dbSNP |