| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.46895805G>A | CA6977703 | HTR2A | c.102C>T (p.Ser34=) c.-78+869C>T (n.-78+869C>T) c.160+869C>T (n.160+869C>T) c.9C>T (p.Ser3=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.46895805G>C | CA483555437 | HTR2A | c.102C>G (p.Ser34=) c.-78+869C>G (n.-78+869C>G) c.160+869C>G (n.160+869C>G) c.9C>G (p.Ser3=) | dbSNP |
| 13 | g.46895805G>T | CA483555438 | HTR2A | c.102C>A (p.Ser34=) c.-78+869C>A (n.-78+869C>A) c.160+869C>A (n.160+869C>A) c.9C>A (p.Ser3=) | dbSNP |
| 13 | g.46895805G= | CA658798137 | HTR2A | c.102C= (p.Ser34=) c.-78+869C= (n.-78+869C=) c.160+869C= (n.160+869C=) c.9C= (p.Ser3=) | ClinVar dbSNP |