List of variants in gene CUBN reported as likely benign by Ambry Genetics

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.10267G>A (p.Val3423Ile)	rs145872906	0.00305
NM_001081.4(CUBN):c.9061G>A (p.Glu3021Lys)	rs41289299	0.00041
NM_001081.4(CUBN):c.3746G>A (p.Arg1249His)	rs151039810	0.00010
NM_001081.4(CUBN):c.2120G>A (p.Arg707His)	rs763524933	0.00006
NM_001081.4(CUBN):c.7300G>A (p.Gly2434Ser)	rs144565631	0.00005
NM_001081.4(CUBN):c.2203G>A (p.Val735Ile)	rs370770104	0.00004
NM_001081.4(CUBN):c.3932G>A (p.Arg1311Gln)	rs1037514591	0.00001
NM_001081.4(CUBN):c.4907G>T (p.Arg1636Leu)	rs538984401	0.00001
NM_001081.4(CUBN):c.2641A>G (p.Ile881Val)
NM_001081.4(CUBN):c.3529A>G (p.Ile1177Val)
NM_001081.4(CUBN):c.6145C>G (p.Gln2049Glu)
NM_001081.4(CUBN):c.6202T>C (p.Tyr2068His)
NM_001081.4(CUBN):c.755T>C (p.Met252Thr)
NM_001081.4(CUBN):c.9001G>A (p.Asp3001Asn)

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