List of variants in gene CUBN reported as uncertain significance for not specified

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.5069C>T (p.Ala1690Val)	rs141640975	0.00155
NM_001081.4(CUBN):c.4376C>G (p.Ser1459Cys)	rs138022214	0.00032
NM_001081.4(CUBN):c.6479A>G (p.Asp2160Gly)	rs144704318	0.00018
NM_001081.4(CUBN):c.6268A>G (p.Lys2090Glu)	rs201374966	0.00010
NM_001081.4(CUBN):c.6613G>A (p.Gly2205Arg)	rs140883483	0.00007
NM_001081.4(CUBN):c.7400A>G (p.Asn2467Ser)	rs200197243	0.00006
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.8909G>A (p.Arg2970His)	rs540096595	0.00001

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