A26G (p.Ala26Gly) variant of KMT2C (Q8NEZ4)
A26G (p.Ala26Gly) in KMT2C (Q8NEZ4) is a missense change. The record also includes variant effect predictions and population frequency data.
A26G (p.Ala26Gly) variant details
- p.Ala26Gly
- TOPMed rs2097911468
- gnomAD rs2097911468
- Missense
- REVEL 0.18
- CADD 22.90
- PolyPhen-2 0.03
- SIFT 0.02
- Most common in the African/African-American population (allele frequency 2.4e-05)