P116H (p.Pro116His) variant of LHCGR (P22888)
P116H (p.Pro116His) in LHCGR (P22888) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. 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.
P116H (p.Pro116His) variant details
- p.Pro116His
- NCI-TCGA Cosmic COSV5430
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.575
- REVEL 0.44
- CADD 24.20
- PolyPhen-2 0.67
- SIFT 0.05
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available