List of variants in gene CUBN reported as uncertain significance by Baylor 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: 6

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HGVS	dbSNP	gnomAD frequency
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.8701G>A (p.Val2901Ile)	rs201093611	0.00004
NM_001081.4(CUBN):c.265A>C (p.Lys89Gln)	rs755860454	0.00001
NM_001081.4(CUBN):c.5305G>C (p.Val1769Leu)	rs74116778
NM_001081.4(CUBN):c.7406C>T (p.Pro2469Leu)	rs202229367

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