E91D (p.Glu91Asp) variant of BIN1 (O00499)
E91D (p.Glu91Asp) in BIN1 (O00499) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E91D (p.Glu91Asp) variant details
- p.Glu91Asp
- NCI-TCGA Cosmic COSV5212
- cosmic curated COSV52120
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available