List of variants in gene PUM1 reported as likely 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001020658.2(PUM1):c.3103A>T (p.Thr1035Ser)	rs771145682	0.00001
NM_001020658.2(PUM1):c.1738C>T (p.Arg580Ter)
NM_001020658.2(PUM1):c.2518C>T (p.Arg840Trp)	rs1640042273
NM_001020658.2(PUM1):c.3242+2T>C

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