S37N (p.Ser37Asn) variant of JUN (Transcription factor Jun)
S37N (p.Ser37Asn) in JUN (Transcription factor Jun) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data.
S37N (p.Ser37Asn) variant details
- p.Ser37Asn
- TOPMed rs1452725173
- gnomAD rs1452725173
- Missense
- Variant Prioritization Score for Impact Estimate 0.275
- REVEL 0.09
- CADD 17.60
- PolyPhen-2 0.01
- SIFT 0.77
- Most common in the REMAINING population (allele frequency 0.00048)