P41S (p.Pro41Ser) variant of FSHR (P23945)
P41S (p.Pro41Ser) in FSHR (P23945) 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 0.86 / 1. The record also includes population frequency data and structural context.
P41S (p.Pro41Ser) variant details
- p.Pro41Ser
- NCI-TCGA Cosmic COSV5863
- cosmic curated COSV58635
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.865
- REVEL 0.89
- MetaLR 0.99
- MetaSVM 0.95
- CADD 24.10
- PolyPhen-2 1.00
- SIFT 0.06
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available