S108I (p.Ser108Ile) variant of PGR (Progesterone receptor)
S108I (p.Ser108Ile) 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 0.23 / 1. The record also includes population frequency data and structural context.
S108I (p.Ser108Ile) variant details
- p.Ser108Ile
- rs1324015244
- NCI-TCGA Cosmic COSV5480
- cosmic curated COSV54804
- TOPMed rs1324015244
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.226
- REVEL 0.05
- CADD 22.90
- PolyPhen-2 0.70
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available