| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.100406916G>C | CA316366 | PCDH19 | c.1682C>G (p.Pro561Arg) | ClinVar dbSNP |
| X | g.100406916G>A | CA414002193 | PCDH19 | c.1682C>T (p.Pro561Leu) | ClinVar dbSNP |
| X | g.100406916G= | CA2447976515 | PCDH19 | c.1682C= (p.Pro561=) | dbSNP |