F6F (p.Phe6Phe) variant of CALCB (P10092)
F6F (p.Phe6Phe) 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.
F6F (p.Phe6Phe) variant details
- p.Phe6Phe
- rs773655356
- gnomAD 11-15074736-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.524
- CADD 15.10
- Most common in the African/African-American population (allele frequency 0.00017)
- Structural context available
- Literature evidence available