Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.69616310T>C | CA261484 | EDA | c.2T>C (p.Met1Thr) n.244T>C n.225T>C | ClinVar dbSNP |
X | g.69616310T>G | CA413446835 | EDA | c.2T>G (p.Met1Arg) n.244T>G n.225T>G | ClinVar dbSNP |
X | g.69616310T= | CA2435839465 | EDA | c.2T= (p.Met1=) n.244T= n.225T= | dbSNP |