P61S (p.Pro61Ser) variant of PGR (Progesterone receptor)
P61S (p.Pro61Ser) in PGR (Progesterone receptor) 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 0.15 / 1. The record also includes population frequency data and structural context.
P61S (p.Pro61Ser) variant details
- p.Pro61Ser
- NCI-TCGA Cosmic COSV9967
- cosmic curated COSV99679
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.152
- REVEL 0.07
- CADD 15.50
- PolyPhen-2 0.01
- SIFT 0.11
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available