M1? variant of ITPR2 (Q14571)
M1? in ITPR2 (Q14571) 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 COSV5438
- NCI-TCGA Cosmic COSV9965
- cosmic curated COSV99659
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available