Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.5302566T>G | CA311167058 | PROKR2 | c.629A>C (p.Gln210Pro) c.521A>C (p.Gln174Pro) | dbSNP gnomAD v2 gnomAD v4 |
20 | g.5302566T>C | CA259600 | PROKR2 | c.629A>G (p.Gln210Arg) c.521A>G (p.Gln174Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.5302566T= | CA2347436481 | PROKR2 | c.629A= (p.Gln210=) c.521A= (p.Gln174=) | dbSNP |