T39N (p.Thr39Asn) variant of JUN (Transcription factor Jun)
T39N (p.Thr39Asn) in JUN (Transcription factor Jun) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and published literature.
T39N (p.Thr39Asn) variant details
- p.Thr39Asn
- gnomAD 1-58782955-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.287
- REVEL 0.08
- MetaLR 0.07
- MetaSVM -1.09
- CADD 21.30
- PolyPhen-2 0.09
- SIFT 0.84
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Literature evidence available