List of variants in gene CUBN reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.10119C>A (p.Val3373=)	rs139596037	0.00168
NM_001081.4(CUBN):c.10105A>G (p.Ser3369Gly)	rs145023719	0.00070
NM_001081.4(CUBN):c.4669C>T (p.Leu1557Phe)	rs140970422	0.00064
NM_001081.4(CUBN):c.7837A>C (p.Ile2613Leu)	rs144626884	0.00031
NM_001081.4(CUBN):c.2738G>C (p.Ser913Thr)	rs201589187	0.00012
NM_001081.4(CUBN):c.4268C>T (p.Thr1423Met)	rs483352704	0.00001
NM_001081.4(CUBN):c.349-6T>A
NM_001081.4(CUBN):c.4838G>T (p.Arg1613Leu)
NM_001081.4(CUBN):c.6764C>T (p.Pro2255Leu)
NM_001081.4(CUBN):c.6916T>C (p.Trp2306Arg)

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