S11N (p.Ser11Asn) variant of JMJD4 (Q9H9V9)
S11N (p.Ser11Asn) in JMJD4 (Q9H9V9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
S11N (p.Ser11Asn) variant details
- p.Ser11Asn
- TOPMed rs960902177
- gnomAD rs960902177
- Missense
- Variant Prioritization Score for Impact Estimate 0.0832
- REVEL 0.03
- ESM-1b 0.00
- AlphaMissense 0.10
- MetaLR 0.02
- MetaSVM -0.98
- CADD 2.43
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available