V16V (p.Val16Val) variant of CALCB (P10092)
V16V (p.Val16Val) in CALCB (P10092) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data, published literature, and structural context.
V16V (p.Val16Val) variant details
- p.Val16Val
- rs1850378108
- gnomAD 11-15074766-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.521
- CADD 14.80
- Most common in the REMAINING population (allele frequency 3.3e-05)
- Structural context available
- Literature evidence available