H49L (p.His49Leu) variant of CHD2 (O14647)
H49L (p.His49Leu) in CHD2 (O14647) is a missense change. The record also includes variant effect predictions and structural context.
H49L (p.His49Leu) variant details
- p.His49Leu
- TOPMed rs1038860028
- Missense
- MetaLR 0.42
- MetaSVM -0.27
- SIFT 0.01
- Structural context available