List of variants in gene ASXL3 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_030632.3(ASXL3):c.3324T>G (p.Ala1108=)	rs77617474	0.00638
NM_030632.3(ASXL3):c.1995A>G (p.Arg665=)	rs143855418	0.00536
NM_030632.3(ASXL3):c.4817G>A (p.Arg1606Gln)	rs116363417	0.00339
NM_030632.3(ASXL3):c.6359C>T (p.Ala2120Val)	rs151081332	0.00217
NM_030632.3(ASXL3):c.6603C>T (p.Ala2201=)	rs3809986	0.00073
NM_030632.3(ASXL3):c.3464C>T (p.Ser1155Leu)	rs377619533	0.00003

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