V6I (p.Val6Ile) variant of SLC2A2 (P11168)
V6I (p.Val6Ile) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
V6I (p.Val6Ile) variant details
- p.Val6Ile
- ExAC rs767313610
- TOPMed rs767313610
- gnomAD rs767313610
- Missense
- Variant Prioritization Score for Impact Estimate 0.123
- REVEL 0.15
- CADD 3.35
- PolyPhen-2 0.00
- SIFT 0.38
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available