G21G (p.Gly21Gly) variant of CALCB (P10092)
G21G (p.Gly21Gly) in CALCB (P10092) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data, published literature, and structural context.
G21G (p.Gly21Gly) variant details
- p.Gly21Gly
- gnomAD 11-15074781-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.401
- CADD 15.50
- Most common in the Non-Finnish European population (allele frequency 5.4e-06)
- Structural context available
- Literature evidence available