Q206* (p.Gln206Ter) variant of MAOB (P27338)
Q206* (p.Gln206Ter) in MAOB (P27338) 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 0.80 / 1. The record also includes population frequency data and structural context.
Q206* (p.Gln206Ter) variant details
- p.Gln206Ter
- NCI-TCGA Cosmic COSV6520
- TOPMed rs2034538269
- Variant assessed as somatic; high impact.
- Stop Gained
- Variant Prioritization Score for Impact Estimate 0.796
- CADD 39.00
- UniProt: Variant assessed as somatic; high impact.
- Most common in the Non-Finnish European population (allele frequency 3.6e-06)
- Structural context available