I69V (p.Ile69Val) variant of SLC2A10 (O95528)
I69V (p.Ile69Val) in SLC2A10 (O95528) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
I69V (p.Ile69Val) variant details
- p.Ile69Val
- NCI-TCGA Cosmic COSV1008
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available