G9S (p.Gly9Ser) variant of SLC2A4 (P14672)
G9S (p.Gly9Ser) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data, published literature, and structural context.
G9S (p.Gly9Ser) variant details
- p.Gly9Ser
- gnomAD 17-7281959-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.342
- REVEL 0.19
- MetaLR 0.27
- MetaSVM -0.79
- CADD 23.40
- PolyPhen-2 0.00
- SIFT 0.23
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available
- Literature evidence available