R37G (p.Arg37Gly) variant of KMT2C (Q8NEZ4)
R37G (p.Arg37Gly) in KMT2C (Q8NEZ4) is a missense change. The record also includes variant effect predictions and population frequency data.
R37G (p.Arg37Gly) variant details
- p.Arg37Gly
- TOPMed rs2097911235
- Missense
- REVEL 0.49
- CADD 24.70
- PolyPhen-2 0.73
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 2.8e-06)