D51G (p.Asp51Gly) variant of SLC2A2 (P11168)
D51G (p.Asp51Gly) in SLC2A2 (P11168) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
D51G (p.Asp51Gly) variant details
- p.Asp51Gly
- NCI-TCGA Cosmic COSV5858
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.284
- REVEL 0.17
- CADD 22.10
- PolyPhen-2 0.18
- SIFT 0.08
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available