List of variants in gene UNG reported as pathogenic for hematologic disorder

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_080911.3(UNG):c.685C>T (p.Arg229Ter)	rs772214871	0.00002
NM_080911.3(UNG):c.162del (p.Gln55fs)
NM_080911.3(UNG):c.250dup (p.Arg84fs)
NM_080911.3(UNG):c.294del (p.Ser97_Trp98insTer)	rs2135882474
NM_080911.3(UNG):c.366_369del (p.Arg122fs)	rs757311287
NM_080911.3(UNG):c.392del (p.Pro131fs)
NM_080911.3(UNG):c.39del (p.Ser14fs)
NM_080911.3(UNG):c.428_429del (p.Ile143fs)
NM_080911.3(UNG):c.569_570del (p.Ile190fs)	rs772764942
NM_080911.3(UNG):c.572_573del (p.Glu191fs)
NM_080911.3(UNG):c.649dup (p.Thr217fs)	rs1302020618
NM_080911.3(UNG):c.730C>T (p.Gln244Ter)	rs751126274
NM_080911.3(UNG):c.752T>C (p.Phe251Ser)	rs104894380

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