S29C (p.Ser29Cys) variant of JUN (Transcription factor Jun)
S29C (p.Ser29Cys) in JUN (Transcription factor Jun) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data.
S29C (p.Ser29Cys) variant details
- p.Ser29Cys
- TOPMed rs1351439445
- gnomAD rs1351439445
- Missense
- Variant Prioritization Score for Impact Estimate 0.24
- REVEL 0.06
- CADD 24.10
- PolyPhen-2 0.75
- SIFT 0.17
- Most common in the African/African-American population (allele frequency 2.4e-05)