| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.35037010C>T | CA3229361 | AGXT2 | c.418G>A (p.Val140Ile) n.327G>A c.415G>A (p.Val139Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.35037010C>A | CA359421044 | AGXT2 | c.418G>T (p.Val140Phe) n.327G>T c.415G>T (p.Val139Phe) | dbSNP |
| 5 | g.35037010C= | CA1538673395 | AGXT2 | c.418G= (p.Val140=) n.327G= c.415G= (p.Val139=) | dbSNP dbSNP |