P33S (p.Pro33Ser) variant of LHCGR (P22888)
P33S (p.Pro33Ser) 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 0.41 / 1. The record also includes population frequency data and structural context.
P33S (p.Pro33Ser) variant details
- p.Pro33Ser
- rs1458995452
- gnomAD rs1458995452
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.409
- REVEL 0.18
- CADD 23.50
- PolyPhen-2 0.00
- SIFT 0.45
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available