R9P (p.Arg9Pro) variant of CDKN1A (P38936)
R9P (p.Arg9Pro) in CDKN1A (P38936) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
R9P (p.Arg9Pro) variant details
- p.Arg9Pro
- NCI-TCGA Cosmic COSV5518
- cosmic curated COSV55187
- 1000Genomes rs143419412
- ESP rs143419412
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.