P97Q (p.Pro97Gln) variant of CALCRL (Q16602)
P97Q (p.Pro97Gln) in CALCRL (Q16602) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data and structural context.
P97Q (p.Pro97Gln) variant details
- p.Pro97Gln
- TOPMed rs974511157
- Missense
- Variant Prioritization Score for Impact Estimate 0.504
- REVEL 0.30
- CADD 26.90
- PolyPhen-2 0.72
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available