List of variants in gene TUFM 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_003321.5(TUFM):c.216_226dup (p.Leu76fs)	rs764459387	0.00001
NC_000016.9:g.(?_28854296)_(28857590_?)del
NM_003321.5(TUFM):c.722dup (p.Leu242fs)

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