| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.100406927G>C | CA121303 | PCDH19 | c.1671C>G (p.Asn557Lys) | ClinVar dbSNP |
| X | g.100406927G>A | CA517747623 | PCDH19 | c.1671C>T (p.Asn557=) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
| X | g.100406927G>T | CA414002219 | PCDH19 | c.1671C>A (p.Asn557Lys) | ClinVar dbSNP |
| X | g.100406927G= | CA2447976520 | PCDH19 | c.1671C= (p.Asn557=) | dbSNP |