V37M (p.Val37Met) variant of CDKN1C (P49918)
V37M (p.Val37Met) in CDKN1C (P49918) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V37M (p.Val37Met) variant details
- p.Val37Met
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available