D151G (p.Asp151Gly) variant of BIN1 (O00499)
D151G (p.Asp151Gly) in BIN1 (O00499) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact in the context of in CNM2. The record also includes structural context.
D151G (p.Asp151Gly) variant details
- p.Asp151Gly
- NCI-TCGA Cosmic COSV9938
- cosmic curated COSV99387
- Variant assessed as somatic; moderate impact.
- in CNM2
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in CNM2)
- Structural context available