S39N (p.Ser39Asn) variant of ID3 (Q02535)
S39N (p.Ser39Asn) in ID3 (Q02535) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
S39N (p.Ser39Asn) variant details
- p.Ser39Asn
- ExAC rs750689669
- TOPMed rs750689669
- gnomAD rs750689669
- Missense
- Variant Prioritization Score for Impact Estimate 0.282
- REVEL 0.08
- MetaLR 0.21
- MetaSVM -0.80
- CADD 22.20
- PolyPhen-2 0.01
- SIFT 0.19
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available