M1? variant of CDKN1A (P38936)
M1? in CDKN1A (P38936) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
M1? variant details
- cosmic curated COSV55188
- NCI-TCGA Cosmic COSV5518
- cosmic curated COSV55187
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.