List of variants in gene ASXL1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 36

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HGVS	dbSNP	gnomAD frequency
NM_015338.6(ASXL1):c.2957A>G (p.Asn986Ser)	rs145132837	0.00172
NM_015338.6(ASXL1):c.3029C>T (p.Thr1010Met)	rs116112525	0.00127
NM_015338.6(ASXL1):c.4189G>A (p.Gly1397Ser)	rs146464648	0.00113
NM_015338.6(ASXL1):c.2059T>C (p.Cys687Arg)	rs140197482	0.00073
NM_015338.6(ASXL1):c.3935C>T (p.Ala1312Val)	rs148144203	0.00073
NM_015338.6(ASXL1):c.1898A>G (p.His633Arg)	rs201280462	0.00069
NM_015338.6(ASXL1):c.4470G>T (p.Leu1490Phe)	rs140896392	0.00057
NM_015338.6(ASXL1):c.1923C>T (p.Ile641=)	rs551524526	0.00042
NM_015338.6(ASXL1):c.4183C>G (p.Leu1395Val)	rs150004862	0.00037
NM_015338.6(ASXL1):c.3933T>C (p.Ala1311=)	rs143779557	0.00032
NM_015338.6(ASXL1):c.3351C>A (p.Pro1117=)	rs373603259	0.00029
NM_015338.6(ASXL1):c.1633C>T (p.Arg545Cys)	rs137920574	0.00028
NM_015338.6(ASXL1):c.1474G>C (p.Ala492Pro)	rs145913172	0.00020
NM_015338.6(ASXL1):c.3148A>G (p.Met1050Val)	rs370804022	0.00019
NM_015338.6(ASXL1):c.4494G>A (p.Thr1498=)	rs138417690	0.00014
NM_015338.6(ASXL1):c.4139C>G (p.Ala1380Gly)	rs139319958	0.00013
NM_015338.6(ASXL1):c.375A>G (p.Val125=)	rs755203412	0.00007
NM_015338.6(ASXL1):c.4247A>G (p.Glu1416Gly)	rs146759903	0.00007
NM_015338.6(ASXL1):c.2053G>A (p.Gly685Arg)	rs369152088	0.00005
NM_015338.6(ASXL1):c.3573T>C (p.Ile1191=)	rs755831609	0.00005
NM_015338.6(ASXL1):c.1200C>T (p.Ala400=)	rs750058388	0.00004
NM_015338.6(ASXL1):c.891G>A (p.Thr297=)	rs758987230	0.00004
NM_015338.6(ASXL1):c.4343A>G (p.Gln1448Arg)	rs772452614	0.00003
NM_015338.6(ASXL1):c.1920C>T (p.Ala640=)	rs532924267	0.00002
NM_015338.6(ASXL1):c.2064G>A (p.Thr688=)	rs202104108	0.00002
NM_015338.6(ASXL1):c.2115G>A (p.Glu705=)	rs767393033	0.00002
NM_015338.6(ASXL1):c.275G>A (p.Arg92His)	rs745960978	0.00002
NM_015338.6(ASXL1):c.4179G>A (p.Leu1393=)	rs201053008	0.00002
NM_015338.6(ASXL1):c.-21CCG[3]	rs764597521
NM_015338.6(ASXL1):c.1113G>A (p.Leu371=)	rs1182540278
NM_015338.6(ASXL1):c.1465C>G (p.Arg489Gly)	rs142172134
NM_015338.6(ASXL1):c.1671C>T (p.Thr557=)	rs372630902
NM_015338.6(ASXL1):c.225T>G (p.Pro75=)
NM_015338.6(ASXL1):c.2895AGG[1] (p.Gly967del)	rs762939072
NM_015338.6(ASXL1):c.2979T>C (p.Ser993=)	rs2145376048
NM_015338.6(ASXL1):c.4521G>A (p.Ala1507=)	rs760605807

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