P36A (p.Pro36Ala) variant of CALCB (P10092)
P36A (p.Pro36Ala) in CALCB (P10092) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data, published literature, and structural context.
P36A (p.Pro36Ala) variant details
- p.Pro36Ala
- gnomAD 11-15075080-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.257
- REVEL 0.09
- CADD 3.20
- PolyPhen-2 0.01
- SIFT 0.67
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available