V58G (p.Val58Gly) variant of CALCB (P10092)
V58G (p.Val58Gly) in CALCB (P10092) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
V58G (p.Val58Gly) variant details
- p.Val58Gly
- gnomAD rs1372157338
- Missense
- Variant Prioritization Score for Impact Estimate 0.308
- REVEL 0.27
- CADD 25.00
- PolyPhen-2 0.77
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 5.4e-06)
- Structural context available