Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.70027937C>A | CA413448337 | EDA | c.607C>A (p.Pro203Thr) c.211C>A (p.Pro71Thr) | ClinVar dbSNP gnomAD v4 |
X | g.70027937C>T | CA261501 | EDA | c.607C>T (p.Pro203Ser) c.211C>T (p.Pro71Ser) | ClinVar dbSNP |
X | g.70027937C= | CA2435979579 | EDA | c.607C= (p.Pro203=) c.211C= (p.Pro71=) | dbSNP |
X | g.70027937C>G | CA413448338 | EDA | c.607C>G (p.Pro203Ala) c.211C>G (p.Pro71Ala) | ClinVar dbSNP |