P60R (p.Pro60Arg) variant of LHCGR (P22888)
P60R (p.Pro60Arg) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data and structural context.
P60R (p.Pro60Arg) variant details
- p.Pro60Arg
- gnomAD rs1268787455
- Missense
- Variant Prioritization Score for Impact Estimate 0.574
- REVEL 0.61
- CADD 22.90
- PolyPhen-2 0.09
- SIFT 0.25
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available