P11S (p.Pro11Ser) variant of PPP2R5D (Q14738)
P11S (p.Pro11Ser) in PPP2R5D (Q14738) 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 0.21 / 1. The record also includes population frequency data and structural context.
P11S (p.Pro11Ser) variant details
- p.Pro11Ser
- rs1181904491
- NCI-TCGA Cosmic COSV5784
- cosmic curated COSV57840
- TOPMed rs1181904491
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.212
- REVEL 0.07
- AlphaMissense 0.06
- MetaLR 0.05
- MetaSVM -1.14
- CADD 14.90
- PolyPhen-2 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available