| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.100407163C>T | CA16621147 | PCDH19 | c.1435G>A (p.Asp479Asn) | ClinVar dbSNP COSMIC |
| X | g.100407163C= | CA2447976613 | PCDH19 | c.1435G= (p.Asp479=) | dbSNP |
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.100407163C>T | CA16621147 | PCDH19 | c.1435G>A (p.Asp479Asn) | ClinVar dbSNP COSMIC |
| X | g.100407163C= | CA2447976613 | PCDH19 | c.1435G= (p.Asp479=) | dbSNP |