L141F (p.Leu141Phe) variant of SLC2A2 (P11168)
L141F (p.Leu141Phe) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
L141F (p.Leu141Phe) variant details
- p.Leu141Phe
- Ensembl rs1715811712
- Missense
- Variant Prioritization Score for Impact Estimate 0.475
- REVEL 0.51
- CADD 23.10
- PolyPhen-2 0.61
- SIFT 0.16
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available