A16T (p.Ala16Thr) variant of JUN (Transcription factor Jun)
A16T (p.Ala16Thr) in JUN (Transcription factor Jun) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data.
A16T (p.Ala16Thr) variant details
- p.Ala16Thr
- rs748223511
- NCI-TCGA Cosmic COSV1009
- ExAC rs748223511
- TOPMed rs748223511
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.374
- REVEL 0.12
- CADD 23.00
- PolyPhen-2 0.15
- SIFT 0.12
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)