| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.43553075T>C | CA9488702 | XRCC1 | c.618A>G (p.Pro206=) c.525A>G (p.Pro175=) c.507A>G (p.Pro169=) n.666A>G c.387-232A>G c.639A>G (p.Pro213=) n.298A>G c.544A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.43553075T>A | CA308774830 | XRCC1 | c.618A>T (p.Pro206=) c.525A>T (p.Pro175=) c.507A>T (p.Pro169=) n.666A>T c.387-232A>T c.639A>T (p.Pro213=) n.298A>T c.544A>T | dbSNP |
| 19 | g.43553075T>G | CA308774843 | XRCC1 | c.618A>C (p.Pro206=) c.525A>C (p.Pro175=) c.507A>C (p.Pro169=) n.666A>C c.387-232A>C c.639A>C (p.Pro213=) n.298A>C c.544A>C | dbSNP |