List of variants reported as pathogenic for Acute myeloid leukemia by Nadeem Sheikh Lab, University of the Punjab

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001754.5(RUNX1):c.161A>T (p.Glu54Val)	rs2058004521
NM_001754.5(RUNX1):c.267G>A (p.Leu89=)	rs2146409992
NM_001754.5(RUNX1):c.320G>A (p.Arg107His)	rs1569084106
NM_002520.7(NPM1):c.875del (p.Lys292fs)	rs2113301331
NM_002520.7(NPM1):c.885A>G (p.Ter295=)	rs2113301391
NM_004364.5(CEBPA):c.1039G>A (p.Glu347Lys)	rs1468313242
NM_004364.5(CEBPA):c.314A>T (p.Asp105Val)	rs2145263100

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.