M74R (p.Met74Arg) variant of SLC2A2 (P11168)
M74R (p.Met74Arg) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
M74R (p.Met74Arg) variant details
- p.Met74Arg
- Ensembl rs1716042516
- Missense
- Variant Prioritization Score for Impact Estimate 0.199
- REVEL 0.30
- CADD 0.01
- PolyPhen-2 0.00
- SIFT 0.55
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available