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
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HGVS dbSNP
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
t(11;17)(q23;q25)

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