Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.100407808C>G | CA414008109 | PCDH19 | c.790G>C (p.Asp264His) | ClinVar dbSNP |
X | g.100407808C>A | CA172968 | PCDH19 | c.790G>T (p.Asp264Tyr) | ClinVar dbSNP |
X | g.100407808C= | CA2447976873 | PCDH19 | c.790G= (p.Asp264=) | dbSNP |