Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.127825259A>T | CA374983163 | ENG | c.242T>A (p.Ile81Asn) c.788T>A (p.Ile263Asn) | ClinVar dbSNP |
9 | g.127825259A>G | CA374983162 | ENG | c.242T>C (p.Ile81Thr) c.788T>C (p.Ile263Thr) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.127825259A>C | CA374983166 | ENG | c.242T>G (p.Ile81Ser) c.788T>G (p.Ile263Ser) | ClinVar dbSNP |