E12D (p.Glu12Asp) variant of SPTBN4 (Q9H254)
E12D (p.Glu12Asp) in SPTBN4 (Q9H254) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E12D (p.Glu12Asp) variant details
- p.Glu12Asp
- NCI-TCGA Cosmic COSV5894
- cosmic curated COSV58948
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available