| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.95171080G>A | CA274274 | FANCC | n.911C>T c.520C>T (p.Arg174Ter) n.578C>T c.665C>T (n.665C>T) n.235C>T c.520C>T (p.Arg174Trp) c.64C>T (p.Arg22Ter) c.64C>T (p.Arg22Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 9 | g.95171080G>T | CA466274629 | FANCC | n.911C>A c.520C>A (p.Arg174=) n.578C>A c.665C>A (n.665C>A) n.235C>A c.64C>A (p.Arg22=) | ClinVar dbSNP gnomAD v4 |
| 9 | g.95171080G>C | CA374338540 | FANCC | n.911C>G c.520C>G (p.Arg174Gly) n.578C>G c.665C>G (n.665C>G) n.235C>G c.64C>G (p.Arg22Gly) | dbSNP |
| 9 | g.95171080G= | CA1865483093 | FANCC | n.911C= c.520C= (p.Arg174=) n.578C= c.665C= (n.665C=) n.235C= c.64C= (p.Arg22=) | dbSNP |