P39Q (p.Pro39Gln) variant of CALCA (P06881)
P39Q (p.Pro39Gln) in CALCA (P06881) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data.
P39Q (p.Pro39Gln) variant details
- p.Pro39Gln
- ExAC rs782622457
- gnomAD rs782622457
- Missense
- Variant Prioritization Score for Impact Estimate 0.0854
- REVEL 0.10
- CADD 0.54
- PolyPhen-2 0.28
- SIFT 0.34
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)