| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.66871368A>C | CA6132226 | PC | c.434T>G (p.Val145Gly) n.290-21303T>G c.314T>G (p.Val105Gly) n.636T>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.66871368A>G | CA339940 | PC | c.434T>C (p.Val145Ala) n.290-21303T>C c.314T>C (p.Val105Ala) n.636T>C | ClinVar dbSNP |
| 11 | g.66871368A>T | CA381502441 | PC | c.434T>A (p.Val145Glu) n.290-21303T>A c.314T>A (p.Val105Glu) n.636T>A | dbSNP |
| 11 | g.66871368A= | CA1979905389 | PC | c.434T= (p.Val145=) n.290-21303T= c.314T= (p.Val105=) n.636T= | dbSNP |