| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.114849062T>C | CA334660364 | HTR2C | c.550+859T>C (n.550+859T>C) c.455+954T>C (n.455+954T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.114849062T>G | CA2452892591 | HTR2C | c.550+859T>G (n.550+859T>G) c.455+954T>G (n.455+954T>G) | dbSNP |
| X | g.114849062T>A | CA1136514853 | HTR2C | c.550+859T>A (n.550+859T>A) c.455+954T>A (n.455+954T>A) | dbSNP gnomAD v3 gnomAD v4 |