| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.230710231G>A | CA1448272 | AGT | c.593C>T (p.Thr198Met) n.1104C>T c.620C>T (p.Thr207Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.230710231G>C | CA345206158 | AGT | c.593C>G (p.Thr198Arg) n.1104C>G c.620C>G (p.Thr207Arg) | dbSNP |
| 1 | g.230710231G>T | CA345206159 | AGT | c.593C>A (p.Thr198Lys) n.1104C>A c.620C>A (p.Thr207Lys) | dbSNP |
| 1 | g.230710231G= | CA1139772873 | AGT | c.593C= (p.Thr198=) n.1104C= c.620C= (p.Thr207=) | dbSNP |