V113W (p.Val113Trp) variant of CDKN1C (P49918)
V113W (p.Val113Trp) in CDKN1C (P49918) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
V113W (p.Val113Trp) variant details
- p.Val113Trp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available