C138G (p.Cys138Gly) variant of ITGA2B (Integrin alpha-IIb)
C138G (p.Cys138Gly) in ITGA2B (Integrin alpha-IIb) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
C138G (p.Cys138Gly) variant details
- p.Cys138Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.89
- MetaSVM 0.80
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available