V137A (p.Val137Ala) variant of SLC2A2 (P11168)
V137A (p.Val137Ala) in SLC2A2 (P11168) 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.
V137A (p.Val137Ala) variant details
- p.Val137Ala
- TOPMed rs993833041
- gnomAD rs993833041
- Missense
- Variant Prioritization Score for Impact Estimate 0.164
- REVEL 0.23
- CADD 0.52
- PolyPhen-2 0.00
- SIFT 0.55
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available