| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.240878086T>A | CA275775 | AGXT | c.1007T>A (p.Val336Asp) n.785T>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.240878086T>C | CA351319581 | AGXT | c.1007T>C (p.Val336Ala) n.785T>C | dbSNP |
| 2 | g.240878086T= | CA1339335784 | AGXT | c.1007T= (p.Val336=) n.785T= | dbSNP |