V148R (p.Val148Arg) variant of BIN1 (O00499)
V148R (p.Val148Arg) in BIN1 (O00499) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
V148R (p.Val148Arg) variant details
- p.Val148Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available