G2S (p.Gly2Ser) variant of CALCB (P10092)
G2S (p.Gly2Ser) in CALCB (P10092) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
G2S (p.Gly2Ser) variant details
- p.Gly2Ser
- Ensembl rs1850377600
- Missense
- Variant Prioritization Score for Impact Estimate 0.362
- REVEL 0.18
- CADD 25.40
- PolyPhen-2 0.52
- SIFT 0.09
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available