V106I (p.Val106Ile) variant of SLC2A2 (P11168)
V106I (p.Val106Ile) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data and structural context.
V106I (p.Val106Ile) variant details
- p.Val106Ile
- TOPMed rs1332764085
- Missense
- Variant Prioritization Score for Impact Estimate 0.106
- REVEL 0.11
- CADD 5.23
- PolyPhen-2 0.03
- SIFT 0.53
- Most common in the Non-Finnish European population (allele frequency 3.6e-06)
- Structural context available