G37C (p.Gly37Cys) variant of JMJD4 (Q9H9V9)
G37C (p.Gly37Cys) in JMJD4 (Q9H9V9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
G37C (p.Gly37Cys) variant details
- p.Gly37Cys
- 1000Genomes rs201199352
- ESP rs201199352
- ExAC rs201199352
- TOPMed rs201199352
- Missense
- Variant Prioritization Score for Impact Estimate 0.165
- REVEL 0.02
- ESM-1b 0.26
- AlphaMissense 0.14
- MetaLR 0.02
- MetaSVM -0.98
- CADD 14.01
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available