W96* (p.Trp96Ter) variant of SLC22A2 (O15244)

Name: SLC22A2 W96* (p.Trp96Ter) variant | CATVariant
Creator: Center for Precision Medicine and Data Sciences
Published: 2026-08-20
License: https://catvariant.com/terms-of-use

W96* (p.Trp96Ter) in SLC22A2 (O15244) 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 0.85 / 1. The record also includes population frequency data and structural context.

W96* (p.Trp96Ter) variant details

p.Trp96Ter
rs896799392
NCI-TCGA Cosmic COSV6526
cosmic curated COSV65267
TOPMed rs896799392
Variant assessed as somatic; high impact.
Stop Gained
Variant Prioritization Score for Impact Estimate 0.852
CADD 37.00
UniProt: Variant assessed as somatic; high impact.
Most common in the Non-Finnish European population (allele frequency 9.9e-06)
Structural context available