R26S (p.Arg26Ser) variant of LHCGR (P22888)
R26S (p.Arg26Ser) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
R26S (p.Arg26Ser) variant details
- p.Arg26Ser
- Ensembl rs1670173866
- Missense
- Variant Prioritization Score for Impact Estimate 0.266
- REVEL 0.12
- CADD 10.20
- PolyPhen-2 0.00
- SIFT 0.43
- Most common in the Finnish in Finland (FIN) population (allele frequency 2.5e-05)
- Structural context available