P97S (p.Pro97Ser) variant of PIK3CD (O00329)
P97S (p.Pro97Ser) in PIK3CD (O00329) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.59 / 1. The record also includes population frequency data and structural context.
P97S (p.Pro97Ser) variant details
- p.Pro97Ser
- TOPMed rs1167794081
- gnomAD rs1167794081
- Missense
- Variant Prioritization Score for Impact Estimate 0.591
- REVEL 0.47
- CADD 23.20
- PolyPhen-2 0.78
- SIFT 0.28
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available