Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.127824960G>T | CA374982821 | ENG | c.285C>A (p.Tyr95Ter) c.831C>A (p.Tyr277Ter) | ClinVar dbSNP |
9 | g.127824960G>A | CA200313119 | ENG | c.285C>T (p.Tyr95=) c.831C>T (p.Tyr277=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.127824960G>C | CA257566 | ENG | c.285C>G (p.Tyr95Ter) c.831C>G (p.Tyr277Ter) | ClinVar dbSNP |