D149G (p.Asp149Gly) variant of BIN1 (O00499)
D149G (p.Asp149Gly) 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.
D149G (p.Asp149Gly) variant details
- p.Asp149Gly
- NCI-TCGA Cosmic COSV9938
- cosmic curated COSV99388
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available