| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.35284953C>G | CA405301171 | HAMP | c.166C>G (p.Arg56Gly) n.2437C>G | dbSNP |
| 19 | g.35284953C>T | CA253053 | HAMP | c.166C>T (p.Arg56Ter) n.2437C>T | ClinVar dbSNP gnomAD v4 COSMIC |
| 19 | g.35284953C= | CA2333586107 | HAMP | c.166C= (p.Arg56=) n.2437C= | dbSNP |