S26Y (p.Ser26Tyr) variant of PIK3CB (P42338)
S26Y (p.Ser26Tyr) in PIK3CB (P42338) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data.
S26Y (p.Ser26Tyr) variant details
- p.Ser26Tyr
- rs760521881
- ClinGen CA2639649
- cosmic curated COSV10517
- ClinVar RCV004209152
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.501
- CADD 23.00
- PolyPhen-2 0.01
- SIFT 0.02
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the REMAINING population (allele frequency 0.00096)