P29S (p.Pro29Ser) variant of VSIR (Q9H7M9)
P29S (p.Pro29Ser) in VSIR (Q9H7M9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
P29S (p.Pro29Ser) variant details
- p.Pro29Ser
- ExAC rs774042928
- TOPMed rs774042928
- gnomAD rs774042928
- Missense
- Variant Prioritization Score for Impact Estimate 0.215
- REVEL 0.05
- CADD 18.20
- PolyPhen-2 0.01
- SIFT 0.72
- Most common in the South Asian population (allele frequency 0.00013)
- Structural context available