S29G (p.Ser29Gly) variant of JUN (Transcription factor Jun)
S29G (p.Ser29Gly) in JUN (Transcription factor Jun) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data.
S29G (p.Ser29Gly) variant details
- p.Ser29Gly
- TOPMed rs1351439445
- gnomAD rs1351439445
- Missense
- Variant Prioritization Score for Impact Estimate 0.197
- REVEL 0.01
- CADD 21.40
- PolyPhen-2 0.00
- SIFT 0.49
- Most common in the African/African-American population (allele frequency 0.00022)