| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.36065988del | CA259978 | WDR62 | c.363del (p.Asp122MetfsTer5) c.447del (p.Asp150MetfsTer5) n.427del n.686del n.454del c.429del (p.Asp144MetfsTer5) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.36065988T= | CA3233714353 | WDR62 | c.363T= (p.Pro121=) c.447T= (p.Pro149=) n.427T= n.686T= n.454T= c.429T= (p.Pro143=) | dbSNP dbSNP |