| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.124405534C>T | CA113971 | OAT | c.550G>A (p.Ala184Thr) n.351G>A n.396G>A c.136G>A (p.Ala46Thr) c.229G>A (p.Ala77Thr) c.-51G>A (n.-51G>A) | ClinVar dbSNP gnomAD v4 |
| 10 | g.124405534C= | CA1942339098 | OAT | c.550G= (p.Ala184=) n.351G= n.396G= c.136G= (p.Ala46=) c.229G= (p.Ala77=) c.-51G= (n.-51G=) | dbSNP |