List of variants in gene PUM1 reported as pathogenic for not provided

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001020658.2(PUM1):c.2352C>G (p.Tyr784Ter)	rs1640047087
NM_001020658.2(PUM1):c.3202C>T (p.Arg1068Ter)
NM_001020658.2(PUM1):c.3439C>T (p.Arg1147Trp)	rs1557539450

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