ClinVar Miner

List of variants in gene ASXL1 reported by Department of Pediatrics, Samsung Medical Center, Samsung Medical Center

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_015338.6(ASXL1):c.4279C>T (p.Pro1427Ser)	rs764162507	0.00001
NM_015338.6(ASXL1):c.3115C>T (p.Gln1039Ter)	rs1221031683

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