| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.100408229G>T | CA316287 | PCDH19 | c.369C>A (p.Asn123Lys) | ClinVar dbSNP |
| X | g.100408229G>A | CA333826100 | PCDH19 | c.369C>T (p.Asn123=) | dbSNP gnomAD v4 COSMIC |
| X | g.100408229G>C | CA414010286 | PCDH19 | c.369C>G (p.Asn123Lys) | ClinVar dbSNP |