A11T (p.Ala11Thr) variant of CALCB (P10092)
A11T (p.Ala11Thr) in CALCB (P10092) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
A11T (p.Ala11Thr) variant details
- p.Ala11Thr
- rs1849704210
- gnomAD 11-14978348-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.0844
- CADD 0.53
- Population evidence available
- Structural context available
- Literature evidence available