ClinVar Miner

List of variants in gene CUBN reported by Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.6479A>G (p.Asp2160Gly)	rs144704318	0.00018
NM_001081.4(CUBN):c.9667T>C (p.Tyr3223His)	rs143533714	0.00017
NM_001081.4(CUBN):c.427A>C (p.Asn143His)	rs151018922	0.00015

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