S42G (p.Ser42Gly) variant of CALCB (P10092)
S42G (p.Ser42Gly) in CALCB (P10092) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
S42G (p.Ser42Gly) variant details
- p.Ser42Gly
- gnomAD rs1850381958
- Missense
- Variant Prioritization Score for Impact Estimate 0.155
- REVEL 0.07
- CADD 15.50
- PolyPhen-2 0.00
- SIFT 0.19
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available