S26C (p.Ser26Cys) variant of G6PC1 (P35575)
S26C (p.Ser26Cys) in G6PC1 (P35575) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
S26C (p.Ser26Cys) variant details
- p.Ser26Cys
- TOPMed rs1337808552
- gnomAD rs1337808552
- Missense
- Variant Prioritization Score for Impact Estimate 0.3
- REVEL 0.12
- CADD 20.20
- PolyPhen-2 0.01
- SIFT 0.16
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available