M1? variant of GRM5 (P41594)
M1? in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
M1? variant details
- NCI-TCGA Cosmic COSV5958
- cosmic curated COSV59587
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.