M95R (p.Met95Arg) variant of SLC2A2 (P11168)
M95R (p.Met95Arg) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
M95R (p.Met95Arg) variant details
- p.Met95Arg
- TOPMed rs1415169647
- gnomAD rs1415169647
- Missense
- Variant Prioritization Score for Impact Estimate 0.469
- REVEL 0.45
- CADD 20.50
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available