Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.107690200G>A | CA261401 | SLC26A4 | c.1226G>A (p.Arg409His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.107690200G>C | CA261402 | SLC26A4 | c.1226G>C (p.Arg409Pro) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.107690200G>T | CA368839267 | SLC26A4 | c.1226G>T (p.Arg409Leu) | ClinVar dbSNP gnomAD v4 |
7 | g.107690200G= | CA1732748383 | SLC26A4 | c.1226G= (p.Arg409=) | dbSNP |