| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.50527611A>C | CA16616783 | TYMP | c.623T>G (p.Val208Gly) c.107T>G (p.Val36Gly) n.742T>G c.334T>G (n.334T>G) c.79T>G c.524T>G (p.Val175Gly) n.748T>G n.910T>G | ClinVar dbSNP |
| 22 | g.50527611A>G | CA412201088 | TYMP | c.623T>C (p.Val208Ala) c.107T>C (p.Val36Ala) n.742T>C c.334T>C (n.334T>C) c.79T>C c.524T>C (p.Val175Ala) n.748T>C n.910T>C | ClinVar dbSNP |
| 22 | g.50527611A= | CA2410908680 | TYMP | c.623T= (p.Val208=) c.107T= (p.Val36=) n.742T= c.334T= (n.334T=) c.79T= c.524T= (p.Val175=) n.748T= n.910T= | dbSNP |