D7N (p.Asp7Asn) variant of CDKN1A (P38936)
D7N (p.Asp7Asn) in CDKN1A (P38936) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
D7N (p.Asp7Asn) variant details
- p.Asp7Asn
- NCI-TCGA Cosmic COSV9978
- cosmic curated COSV99781
- Ensembl rs2150312746
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.