| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.100407263G>T | CA316348 | PCDH19 | c.1335C>A (p.Asp445Glu) | ClinVar dbSNP |
| X | g.100407263G>C | CA16616395 | PCDH19 | c.1335C>G (p.Asp445Glu) | ClinVar dbSNP |
| X | g.100407263G= | CA2447976656 | PCDH19 | c.1335C= (p.Asp445=) | dbSNP |