Q19* (p.Gln19Ter) variant of SLC22A2 (O15244)

Name: SLC22A2 Q19* (p.Gln19Ter) variant | CATVariant
Creator: Center for Precision Medicine and Data Sciences
Published: 2026-08-20
License: https://catvariant.com/terms-of-use

Q19* (p.Gln19Ter) 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.

Q19* (p.Gln19Ter) variant details

p.Gln19Ter
NCI-TCGA Cosmic COSV6526
Variant assessed as somatic; high impact.
Stop Gained
Variant Prioritization Score for Impact Estimate 0.849
CADD 37.00
UniProt: Variant assessed as somatic; high impact.
Most common in the Non-Finnish European population (allele frequency 1.8e-06)
Structural context available