Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.203868002G>A | CA10602845 | CTLA4 | c.60G>A (p.Trp20Ter) c.132G>A (p.Trp44Ter) n.60G>A n.200G>A | ClinVar dbSNP |
2 | g.203868002G= | CA1322148604 | CTLA4 | c.60G= (p.Trp20=) c.132G= (p.Trp44=) n.60G= n.200G= | dbSNP |