D37G (p.Asp37Gly) variant of CALCB (P10092)
D37G (p.Asp37Gly) in CALCB (P10092) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data and structural context.
D37G (p.Asp37Gly) variant details
- p.Asp37Gly
- Ensembl rs1850381603
- Missense
- Variant Prioritization Score for Impact Estimate 0.366
- REVEL 0.29
- CADD 23.80
- PolyPhen-2 0.99
- SIFT 0.06
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available