| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.144415027G>A | CA187649376 | SLC39A4 | c.751C>T (p.Arg251Trp) c.676C>T (p.Arg226Trp) c.469C>T (p.Arg157Trp) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.144415027G>T | CA1826307522 | SLC39A4 | c.751C>A (p.Arg251=) c.676C>A (p.Arg226=) c.469C>A (p.Arg157=) | dbSNP |
| 8 | g.144415027G>C | CA372622627 | SLC39A4 | c.751C>G (p.Arg251Gly) c.676C>G (p.Arg226Gly) c.469C>G (p.Arg157Gly) | dbSNP |