L37P (p.Leu37Pro) variant of CDKN1A (P38936)
L37P (p.Leu37Pro) in CDKN1A (P38936) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
L37P (p.Leu37Pro) variant details
- p.Leu37Pro
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available