W7* (p.Trp7Ter) variant of GRIN2A (Q12879)
W7* (p.Trp7Ter) in GRIN2A (Q12879) is a protein-truncating change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.84 / 1. The record also includes population frequency data and structural context.
W7* (p.Trp7Ter) variant details
- p.Trp7Ter
- rs1555491564
- NCI-TCGA Cosmic COSV1004
- NCI-TCGA Cosmic COSV5804
- cosmic curated COSV58041
- Variant assessed as somatic; high impact.
- Stop Gained
- Variant Prioritization Score for Impact Estimate 0.838
- CADD 36.00
- UniProt: Variant assessed as somatic; high impact.
- Population evidence available
- Structural context available