G89W (p.Gly89Trp) variant of SPTA1 (P02549)
G89W (p.Gly89Trp) in SPTA1 (P02549) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
G89W (p.Gly89Trp) variant details
- p.Gly89Trp
- NCI-TCGA Cosmic COSV6375
- cosmic curated COSV63753
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.