G13R (p.Gly13Arg) variant of SLC2A4 (P14672)
G13R (p.Gly13Arg) 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.
G13R (p.Gly13Arg) variant details
- p.Gly13Arg
- gnomAD 17-7283248-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.384
- REVEL 0.16
- MetaLR 0.27
- MetaSVM -0.69
- CADD 22.60
- PolyPhen-2 0.00
- SIFT 0.14
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available