List of variants in gene ASXL1 reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_015338.6(ASXL1):c.472-22T>C	rs4911230	0.02677
NM_015338.6(ASXL1):c.374-9C>T	rs6087903	0.01488
NM_015338.6(ASXL1):c.565+211T>C	rs7260822	0.01035
NM_015338.6(ASXL1):c.3498C>G (p.Ser1166Arg)	rs75887545	0.00728
NM_015338.6(ASXL1):c.3513G>A (p.Arg1171=)	rs150391716	0.00538
NM_015338.6(ASXL1):c.2957A>G (p.Asn986Ser)	rs145132837	0.00172
NM_015338.6(ASXL1):c.252+11T>C	rs143337375	0.00128
NM_015338.6(ASXL1):c.3029C>T (p.Thr1010Met)	rs116112525	0.00127
NM_015338.6(ASXL1):c.3739C>T (p.Arg1247Cys)	rs146747814	0.00113
NM_015338.6(ASXL1):c.4189G>A (p.Gly1397Ser)	rs146464648	0.00113
NM_015338.6(ASXL1):c.3889G>A (p.Val1297Ile)	rs140137262	0.00055
NM_015338.6(ASXL1):c.2820G>A (p.Leu940=)	rs201554973	0.00006
NM_015338.6(ASXL1):c.592G>A (p.Glu198Lys)	rs376793343	0.00006
NM_015338.6(ASXL1):c.2670C>T (p.Leu890=)	rs140299198	0.00003
NM_015338.6(ASXL1):c.2110G>A (p.Gly704Arg)	rs151317625
NM_015338.6(ASXL1):c.57+19G>A	rs200198574

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