S42S (p.Ser42Ser) variant of CALCB (P10092)
S42S (p.Ser42Ser) in CALCB (P10092) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data, published literature, and structural context.
S42S (p.Ser42Ser) variant details
- p.Ser42Ser
- rs143189175
- gnomAD 11-15075100-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.141
- CADD 8.56
- Most common in the 1KG:CLM population (allele frequency 0.0053)
- Structural context available
- Literature evidence available