R39W (p.Arg39Trp) variant of KMT2C (Q8NEZ4)
R39W (p.Arg39Trp) in KMT2C (Q8NEZ4) is a missense change. The record also includes variant effect predictions and population frequency data.
R39W (p.Arg39Trp) variant details
- p.Arg39Trp
- TOPMed rs2097911172
- gnomAD rs2097911172
- Missense
- REVEL 0.53
- CADD 26.00
- PolyPhen-2 0.88
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.9e-06)