E59K (p.Glu59Lys) variant of ASH1L (Q9NR48)
E59K (p.Glu59Lys) in ASH1L (Q9NR48) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes variant effect predictions, population frequency data, and published literature.
E59K (p.Glu59Lys) variant details
- p.Glu59Lys
- rs1668873954
- ClinGen CA342715431
- ClinVar RCV002892067
- NCI-TCGA TCGA novel
- Uncertain significance
- Inborn genetic diseases
- Missense
- REVEL 0.30
- CADD 18.00
- PolyPhen-2 0.02
- SIFT 0.04
- ClinVar: Uncertain significance (Inborn genetic diseases)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 4.4e-05)
- Cited in: Specific guidelines for assessing and improving the methodological quality of economic evaluations of newborn screening. (PMID 22947299)
- Cited in: Including the initial newborn screening bloodspot collection device serial number on birth certificates: basis and… (PMID 23037933)