List of variants in gene CUBN reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.2756A>G (p.His919Arg)	rs148869805	0.00464
NM_001081.4(CUBN):c.5069C>T (p.Ala1690Val)	rs141640975	0.00155
NM_001081.4(CUBN):c.8894T>C (p.Phe2965Ser)	rs117620008	0.00133
NM_001081.4(CUBN):c.3356T>C (p.Leu1119Ser)	rs141164907	0.00089
NM_001081.4(CUBN):c.6263T>C (p.Phe2088Ser)	rs74844886	0.00029
NM_001081.4(CUBN):c.5926+5G>A	rs143301088	0.00019
NM_001081.4(CUBN):c.6479A>G (p.Asp2160Gly)	rs144704318	0.00019
NM_001081.4(CUBN):c.9418G>A (p.Ala3140Thr)	rs148491916	0.00014
NM_001081.4(CUBN):c.6268A>G (p.Lys2090Glu)	rs201374966	0.00010
NM_001081.4(CUBN):c.6613G>A (p.Gly2205Arg)	rs140883483	0.00008
NM_001081.4(CUBN):c.7400A>G (p.Asn2467Ser)	rs200197243	0.00006
NM_001081.4(CUBN):c.1719A>T (p.Leu573Phe)	rs148313915	0.00004
NM_001081.4(CUBN):c.5957A>T (p.Asp1986Val)	rs772570411	0.00004
NM_001081.4(CUBN):c.4268C>T (p.Thr1423Met)	rs483352704	0.00001
NM_001081.4(CUBN):c.8720C>A (p.Ala2907Glu)	rs758557930	0.00001
NM_001081.4(CUBN):c.5840C>A (p.Ser1947Tyr)	rs147617753

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