A11G (p.Ala11Gly) variant of CALCB (P10092)
A11G (p.Ala11Gly) in CALCB (P10092) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data, published literature, and structural context.
A11G (p.Ala11Gly) variant details
- p.Ala11Gly
- rs574877649
- gnomAD 11-14978349-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.186
- CADD 3.67
- Population evidence available
- Structural context available
- Literature evidence available