| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.69098620T>C | CA2944699 | UGT2B11,UGT2B7 | c.802T>C (p.Tyr268His) c.55T>C (p.Tyr19His) n.340T>C c.*106-93867A>G (n.*106-93867A>G) c.*380-93867A>G (n.*380-93867A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.69098620T= | CA1466050307 | UGT2B11,UGT2B7 | c.802T= (p.Tyr268=) c.55T= (p.Tyr19=) n.340T= c.*106-93867A= (n.*106-93867A=) c.*380-93867A= (n.*380-93867A=) | dbSNP |