I99V (p.Ile99Val) variant of SLC2A4 (P14672)
I99V (p.Ile99Val) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and structural context.
I99V (p.Ile99Val) variant details
- p.Ile99Val
- ExAC rs754025923
- gnomAD rs754025923
- cosmic curated COSV50301
- Missense
- Variant Prioritization Score for Impact Estimate 0.139
- REVEL 0.12
- CADD 12.10
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available