W16* (p.Trp16Ter) variant of ADH1B (P00325)
W16* (p.Trp16Ter) in ADH1B (P00325) 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 0.82 / 1. The record also includes population frequency data and structural context.
W16* (p.Trp16Ter) variant details
- p.Trp16Ter
- rs1453332261
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10052
- gnomAD rs1453332261
- Variant assessed as somatic; high impact.
- Stop Gained
- Variant Prioritization Score for Impact Estimate 0.821
- CADD 35.00
- UniProt: Variant assessed as somatic; high impact.
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available