G68V (p.Gly68Val) variant of SLC2A4 (P14672)
G68V (p.Gly68Val) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
G68V (p.Gly68Val) variant details
- p.Gly68Val
- ESP rs144936940
- ExAC rs144936940
- TOPMed rs144936940
- gnomAD rs144936940
- Missense
- Variant Prioritization Score for Impact Estimate 0.397
- REVEL 0.23
- CADD 21.20
- PolyPhen-2 0.01
- SIFT 0.53
- Most common in the African/African-American population (allele frequency 7.2e-05)
- Structural context available