V101A (p.Val101Ala) variant of SLC2A2 (P11168)
V101A (p.Val101Ala) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.73 / 1. The record also includes population frequency data and structural context.
V101A (p.Val101Ala) variant details
- p.Val101Ala
- ExAC rs770135219
- gnomAD rs770135219
- Missense
- Variant Prioritization Score for Impact Estimate 0.733
- REVEL 0.79
- CADD 27.30
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available