P38S (p.Pro38Ser) variant of LHCGR (P22888)
P38S (p.Pro38Ser) 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 0.25 / 1. The record also includes population frequency data and structural context.
P38S (p.Pro38Ser) variant details
- p.Pro38Ser
- NCI-TCGA Cosmic COSV9968
- cosmic curated COSV99683
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.248
- REVEL 0.12
- CADD 17.00
- PolyPhen-2 0.06
- SIFT 0.91
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available