Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.128912083T>C | CA477704110 | KCNJ5 | c.810T>C (p.Leu270=) | ClinVar dbSNP |
11 | g.128912083T>A | CA477704109 | KCNJ5 | c.810T>A (p.Leu270=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.128912083T>G | CA291752 | KCNJ5 | c.810T>G (p.Leu270=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |