Q17* (p.Gln17Ter) variant of SLC2A4 (P14672)
Q17* (p.Gln17Ter) in SLC2A4 (P14672) 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 0.84 / 1. The record also includes population frequency data and structural context.
Q17* (p.Gln17Ter) variant details
- p.Gln17Ter
- rs1420669714
- gnomAD rs1420669714
- Variant assessed as somatic; high impact.
- Stop Gained
- Variant Prioritization Score for Impact Estimate 0.845
- CADD 35.00
- UniProt: Variant assessed as somatic; high impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available