S15G (p.Ser15Gly) variant of PCCB (P05166)
S15G (p.Ser15Gly) in PCCB (P05166) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
S15G (p.Ser15Gly) variant details
- p.Ser15Gly
- gnomAD rs1941477368
- Missense
- Variant Prioritization Score for Impact Estimate 0.205
- REVEL 0.26
- ESM-1b 0.00
- AlphaMissense 0.07
- CADD 10.80
- PolyPhen-2 0.01
- SIFT 0.09
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available