| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.152304695del | CA16616972 | FLG | c.10191del (p.Glu3397AspfsTer?) c.9109-862del (n.9109-862del) | ClinVar dbSNP |
| 1 | g.152304695C= | CA1147188142 | FLG | c.10191G= (p.Glu3397=) c.9109-862G= (n.9109-862G=) | dbSNP dbSNP |