G37S (p.Gly37Ser) variant of JMJD4 (Q9H9V9)
G37S (p.Gly37Ser) in JMJD4 (Q9H9V9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
G37S (p.Gly37Ser) variant details
- p.Gly37Ser
- 1000Genomes rs201199352
- ESP rs201199352
- ExAC rs201199352
- TOPMed rs201199352
- Missense
- Variant Prioritization Score for Impact Estimate 0.149
- REVEL 0.04
- ESM-1b 0.00
- AlphaMissense 0.09
- MetaLR 0.01
- MetaSVM -0.99
- CADD 11.38
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.025)
- Structural context available