Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.240878721G>A | CA275783 | AGXT | c.1079G>A (p.Arg360Gln) n.857G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.240878721G>C | CA351319729 | AGXT | c.1079G>C (p.Arg360Pro) n.857G>C | ClinVar dbSNP |
2 | g.240878721G>T | CA351319730 | AGXT | c.1079G>T (p.Arg360Leu) n.857G>T | dbSNP gnomAD v4 |
2 | g.240878721G= | CA1339336121 | AGXT | c.1079G= (p.Arg360=) n.857G= | dbSNP |