List of variants in gene UBR4 reported as uncertain significance by Medical Research Institute, Tokyo Medical and Dental University

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_020765.3(UBR4):c.6397G>A (p.Ala2133Thr)	rs539999527	0.00001
NM_020765.3(UBR4):c.1097A>G (p.Lys366Arg)	rs796052208
NM_020765.3(UBR4):c.1349G>T (p.Arg450Leu)	rs757121959
NM_020765.3(UBR4):c.1557G>C (p.Gln519His)	rs796052209

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