| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.20999754T>G | CA7084761 | SLC39A2 | c.128T>G (p.Leu43Arg) n.284T>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.20999754T>A | CA7084762 | SLC39A2 | c.128T>A (p.Leu43Gln) n.284T>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.20999754T= | CA2122299508 | SLC39A2 | c.128T= (p.Leu43=) n.284T= | dbSNP |