| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.46897343C>T | CA13844405 | HTR2A | c.-329+609G>A (n.-329+609G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.46897343C>A | CA2018007898 | HTR2A | c.-329+609G>T (n.-329+609G>T) | dbSNP |
| 13 | g.46897343C= | CA2018007897 | HTR2A | c.-329+609G= (n.-329+609G=) | dbSNP |