C151* (p.Cys151Ter) variant of COMP (P49747)
C151* (p.Cys151Ter) in COMP (P49747) 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 0.40 / 1. The record also includes population frequency data and structural context.
C151* (p.Cys151Ter) variant details
- p.Cys151Ter
- rs201389713
- NCI-TCGA Cosmic COSV9972
- cosmic curated COSV99721
- 1000Genomes rs201389713
- Variant assessed as somatic; high impact.
- Stop Gained
- Variant Prioritization Score for Impact Estimate 0.396
- CADD 36.00
- UniProt: Variant assessed as somatic; high impact.
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available