Q55L (p.Gln55Leu) variant of CALCB (P10092)
Q55L (p.Gln55Leu) in CALCB (P10092) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
Q55L (p.Gln55Leu) variant details
- p.Gln55Leu
- ESP rs372815579
- TOPMed rs372815579
- gnomAD rs372815579
- Missense
- Variant Prioritization Score for Impact Estimate 0.287
- REVEL 0.12
- CADD 23.90
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available