R26H (p.Arg26His) variant of LHCGR (P22888)
R26H (p.Arg26His) 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 0.26 / 1. The record also includes population frequency data and structural context.
R26H (p.Arg26His) variant details
- p.Arg26His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.259
- REVEL 0.12
- CADD 6.36
- PolyPhen-2 0.00
- SIFT 0.55
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available