ClinVar Miner

List of variants reported as pathogenic for acute leukemia of ambiguous lineage

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
Download table as spreadsheet
NC_000001.11:g.198807802C>A rs9660525
NM_000314.7(PTEN):c.406T>C (p.Cys136Arg) rs786201044
NM_000546.5(TP53):c.636del (p.Arg213fs) rs864309495
NM_000551.3(VHL):c.598C>T (p.Arg200Trp) rs28940298
NM_002049.3(GATA1):c.154_173dup (p.Ala59fs) rs398124628
NR_040073.1(MIR181A1HG):n.363+1456C>T rs10800597
NR_040073.1(MIR181A1HG):n.363+1862C>A rs60639710
NR_040073.1(MIR181A1HG):n.363+26A>G rs10800598
NR_040073.1(MIR181A1HG):n.364-18748G>A rs12406470

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.