G61W (p.Gly61Trp) variant of ASH1L (Q9NR48)
G61W (p.Gly61Trp) in ASH1L (Q9NR48) is a missense change. The record also includes variant effect predictions and population frequency data.
G61W (p.Gly61Trp) variant details
- p.Gly61Trp
- TOPMed rs1244265447
- gnomAD rs1244265447
- Missense
- REVEL 0.43
- CADD 23.70
- PolyPhen-2 0.77
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)