| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.124402930G>C | CA113998 | OAT | c.897C>G (p.Tyr299Ter) n.698C>G n.407C>G c.483C>G (p.Tyr161Ter) c.576C>G (p.Tyr192Ter) c.297C>G (p.Tyr99Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.124402930G>A | CA471762770 | OAT | c.897C>T (p.Tyr299=) n.698C>T n.407C>T c.483C>T (p.Tyr161=) c.576C>T (p.Tyr192=) c.297C>T (p.Tyr99=) | ClinVar dbSNP COSMIC |
| 10 | g.124402930G= | CA1942337905 | OAT | c.897C= (p.Tyr299=) n.698C= n.407C= c.483C= (p.Tyr161=) c.576C= (p.Tyr192=) c.297C= (p.Tyr99=) | dbSNP |