List of variants in gene ASXL1 reported as uncertain significance for not specified

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_015338.6(ASXL1):c.1205G>A (p.Arg402Gln)	rs755749479	0.00005
NM_015338.6(ASXL1):c.3102A>T (p.Lys1034Asn)	rs751952846	0.00001
NM_015338.6(ASXL1):c.314C>T (p.Thr105Met)	rs749495615	0.00001
NM_015338.6(ASXL1):c.4308C>G (p.Ile1436Met)	rs748596785	0.00001
NM_015338.6(ASXL1):c.1246C>T (p.Leu416Phe)
NM_015338.6(ASXL1):c.2550A>T (p.Glu850Asp)
NM_015338.6(ASXL1):c.3370C>G (p.Pro1124Ala)	rs758338148
NM_015338.6(ASXL1):c.3635C>T (p.Ser1212Phe)	rs542568224

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