M1? variant of PRMT5 (O14744)
M1? in PRMT5 (O14744) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
M1? variant details
- NCI-TCGA Cosmic COSV5354
- cosmic curated COSV53545
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available