V32= variant of ARAF (P10398)
V32= in ARAF (P10398) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; low impact. The record also includes experimental measurements and structural context.
V32= variant details
- NCI-TCGA TCGA novel
- Variant assessed as somatic; low impact.
- Missense
- UniProt: Variant assessed as somatic; low impact.
- Structural context available
- ARAF Raf-like Ras-binding domain domainome 1.0: score -0.0122