A11S (p.Ala11Ser) variant of CALCB (P10092)
A11S (p.Ala11Ser) 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.
A11S (p.Ala11Ser) variant details
- p.Ala11Ser
- gnomAD 11-14978348-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.0822
- CADD 0.22
- Population evidence available
- Structural context available
- Literature evidence available