V16F (p.Val16Phe) variant of CALCB (P10092)
V16F (p.Val16Phe) in CALCB (P10092) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
V16F (p.Val16Phe) variant details
- p.Val16Phe
- gnomAD rs1255798853
- Missense
- Variant Prioritization Score for Impact Estimate 0.317
- REVEL 0.21
- CADD 23.90
- PolyPhen-2 0.76
- SIFT 0.05
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available