Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.107683537G>C | CA4432642 | SLC26A4 | c.1001G>C (p.Gly334Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.107683537G>T | CA274302 | SLC26A4 | c.1001G>T (p.Gly334Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.107683537G>A | CA164205791 | SLC26A4 | c.1001G>A (p.Gly334Glu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |