R51C (p.Arg51Cys) variant of SLC2A1 (P11166)
R51C (p.Arg51Cys) in SLC2A1 (P11166) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance in the context of in EIG12. The record also includes structural context.
R51C (p.Arg51Cys) variant details
- p.Arg51Cys
- NCI-TCGA Cosmic COSV6528
- TOPMed rs1643485589
- Uncertain significance
- in EIG12
- Missense
- EBI: uncertain significance (in EIG12)
- UniProt: Uncertain significance (in EIG12)
- Structural context available