| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.67365493G>A | CA6136128 | CLCF1,RAD9A | c.321C>T (p.Tyr107=) c.291C>T (p.Tyr97=) c.16+8031C>T (n.16+8031C>T) n.392-22042G>A n.424-22042G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.67365493G>T | CA340027 | CLCF1,RAD9A | c.321C>A (p.Tyr107Ter) c.291C>A (p.Tyr97Ter) c.16+8031C>A (n.16+8031C>A) n.392-22042G>T n.424-22042G>T | ClinVar dbSNP |