V25D (p.Val25Asp) variant of SLC2A4 (P14672)
V25D (p.Val25Asp) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data, published literature, and structural context.
V25D (p.Val25Asp) variant details
- p.Val25Asp
- gnomAD 17-7283285-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.512
- REVEL 0.52
- CADD 23.80
- PolyPhen-2 0.24
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available