Y18Y (p.Tyr18Tyr) variant of CALCB (P10092)
Y18Y (p.Tyr18Tyr) in CALCB (P10092) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data, published literature, and structural context.
Y18Y (p.Tyr18Tyr) variant details
- p.Tyr18Tyr
- gnomAD 11-15074772-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.501
- CADD 12.70
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available