| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.9743637G>T | CA226190 | GPR143 | c.695C>A (p.Thr232Lys) c.443C>A (p.Thr148Lys) | ClinVar dbSNP gnomAD v4 |
| X | g.9743637G>A | CA10344958 | GPR143 | c.695C>T (p.Thr232Met) c.443C>T (p.Thr148Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| X | g.9743637G= | CA2415025113 | GPR143 | c.695C= (p.Thr232=) c.443C= (p.Thr148=) | dbSNP |