G22W (p.Gly22Trp) variant of SLC2A4 (P14672)
G22W (p.Gly22Trp) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data, published literature, and structural context.
G22W (p.Gly22Trp) variant details
- p.Gly22Trp
- gnomAD 17-7283275-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.377
- REVEL 0.25
- CADD 24.10
- PolyPhen-2 0.76
- SIFT 0.17
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available