| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.79171491T>A | CA10460874 | GPR174 | c.484T>A (p.Ser162Thr) n.760+14573T>A n.777+14573T>A n.756+14573T>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.79171491T>G | CA413736119 | GPR174 | c.484T>G (p.Ser162Ala) n.760+14573T>G n.777+14573T>G n.756+14573T>G | dbSNP |
| X | g.79171491T>C | CA10460873 | GPR174 | c.484T>C (p.Ser162Pro) n.760+14573T>C n.777+14573T>C n.756+14573T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |