L67V (p.Leu67Val) variant of SLC2A2 (P11168)
L67V (p.Leu67Val) 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.
L67V (p.Leu67Val) variant details
- p.Leu67Val
- gnomAD rs1716046696
- Missense
- Variant Prioritization Score for Impact Estimate 0.112
- REVEL 0.15
- CADD 0.18
- PolyPhen-2 0.01
- SIFT 0.43
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available