Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.66870409A>C | CA16606005 | PC | c.796T>G (p.Ser266Ala) n.290-20344T>G c.676T>G (p.Ser226Ala) | ClinVar dbSNP gnomAD v4 |
11 | g.66870409A>G | CA6132104 | PC | c.796T>C (p.Ser266Pro) n.290-20344T>C c.676T>C (p.Ser226Pro) | dbSNP ExAC gnomAD v2 |
11 | g.66870409A>T | CA341775 | PC | c.796T>A (p.Ser266Thr) n.290-20344T>A c.676T>A (p.Ser226Thr) | dbSNP |