List of variants in gene CUBN reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.8894T>C (p.Phe2965Ser)	rs117620008	0.00133
NM_001081.4(CUBN):c.8593G>A (p.Val2865Met)	rs146847375	0.00037
NM_001081.4(CUBN):c.6091A>G (p.Thr2031Ala)	rs150392211	0.00034
NM_001081.4(CUBN):c.814G>A (p.Gly272Arg)	rs146035059	0.00029
NM_001081.4(CUBN):c.9079G>A (p.Gly3027Arg)	rs150202444	0.00021
NM_001081.4(CUBN):c.6020C>T (p.Thr2007Met)	rs140202552	0.00019
NM_001081.4(CUBN):c.3995A>G (p.Asn1332Ser)	rs370803308	0.00017
NM_001081.4(CUBN):c.323G>A (p.Ser108Asn)	rs543983858	0.00010
NM_001081.4(CUBN):c.6613G>A (p.Gly2205Arg)	rs140883483	0.00008
NM_001081.4(CUBN):c.1030G>A (p.Gly344Arg)
NM_001081.4(CUBN):c.10729G>T (p.Ala3577Ser)	rs139051724
NM_001081.4(CUBN):c.4148A>G (p.Gln1383Arg)
NM_001081.4(CUBN):c.4656C>T (p.Phe1552=)	rs2131697240
NM_001081.4(CUBN):c.4720A>G (p.Met1574Val)	rs1482983523
NM_001081.4(CUBN):c.5056G>A (p.Gly1686Ser)
NM_001081.4(CUBN):c.5840C>A (p.Ser1947Tyr)	rs147617753
NM_001081.4(CUBN):c.9199A>G (p.Thr3067Ala)

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