| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.144414422C>T | CA116337 | SLC39A4 | c.989G>A (p.Gly330Asp) c.914G>A (p.Gly305Asp) c.707G>A (p.Gly236Asp) | ClinVar dbSNP gnomAD v4 |
| 8 | g.144414422C>A | CA372621388 | SLC39A4 | c.989G>T (p.Gly330Val) c.914G>T (p.Gly305Val) c.707G>T (p.Gly236Val) | dbSNP gnomAD v4 |
| 8 | g.144414422C= | CA1826307158 | SLC39A4 | c.989G= (p.Gly330=) c.914G= (p.Gly305=) c.707G= (p.Gly236=) | dbSNP |