Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.107663412C>T | CA16041101 | SLC26A4 | c.281C>T (p.Thr94Ile) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.107663412C>G | CA368845720 | SLC26A4 | c.281C>G (p.Thr94Ser) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.107663412C= | CA1732736183 | SLC26A4 | c.281C= (p.Thr94=) | dbSNP |