I71M (p.Ile71Met) variant of SLC2A1 (P11166)
I71M (p.Ile71Met) in SLC2A1 (P11166) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
I71M (p.Ile71Met) variant details
- p.Ile71Met
- NCI-TCGA Cosmic COSV6528
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available