G33D (p.Gly33Asp) variant of SMARCA4 (P51532)
G33D (p.Gly33Asp) in SMARCA4 (P51532) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G33D (p.Gly33Asp) variant details
- p.Gly33Asp
- NCI-TCGA Cosmic COSV6079
- cosmic curated COSV60791
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available