| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.107674970G>T | CA253304 | SLC26A4 | c.626G>T (p.Gly209Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.107674970G= | CA1732746914 | SLC26A4 | c.626G= (p.Gly209=) | dbSNP |
| 7 | g.107674970G>A | CA368831124 | SLC26A4 | c.626G>A (p.Gly209Glu) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.107674970G>C | CA368831126 | SLC26A4 | c.626G>C (p.Gly209Ala) | dbSNP gnomAD v4 |