Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.240878718T>C | CA275781 | AGXT | c.1076T>C (p.Leu359Pro) n.854T>C | ClinVar dbSNP gnomAD v4 |
2 | g.240878718T>G | CA351319727 | AGXT | c.1076T>G (p.Leu359Arg) n.854T>G | dbSNP gnomAD v4 |
2 | g.240878718T= | CA1339336118 | AGXT | c.1076T= (p.Leu359=) n.854T= | dbSNP |