I42M (p.Ile42Met) variant of SLC2A4 (P14672)
I42M (p.Ile42Met) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
I42M (p.Ile42Met) variant details
- p.Ile42Met
- gnomAD rs1277048692
- Missense
- Variant Prioritization Score for Impact Estimate 0.302
- REVEL 0.34
- CADD 22.60
- PolyPhen-2 0.64
- SIFT 0.03
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available