S7S (p.Ser7Ser) variant of CALCB (P10092)
S7S (p.Ser7Ser) in CALCB (P10092) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
S7S (p.Ser7Ser) variant details
- p.Ser7Ser
- rs766953127
- gnomAD 11-15074739-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.15
- CADD 9.37
- Most common in the East Asian population (allele frequency 5e-05)
- Structural context available
- Literature evidence available