I94T (p.Ile94Thr) variant of SLC2A4 (P14672)
I94T (p.Ile94Thr) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data and structural context.
I94T (p.Ile94Thr) variant details
- p.Ile94Thr
- TOPMed rs1430231976
- gnomAD rs1430231976
- Missense
- Variant Prioritization Score for Impact Estimate 0.623
- REVEL 0.63
- CADD 24.20
- PolyPhen-2 0.38
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available