List of variants in gene CUBN reported as uncertain significance for CUBN-related condition

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.6125-2A>G	rs75386064	0.00226
NM_001081.4(CUBN):c.8894T>C (p.Phe2965Ser)	rs117620008	0.00133
NM_001081.4(CUBN):c.6260C>G (p.Ser2087Cys)	rs376641725	0.00016
NM_001081.4(CUBN):c.6187C>T (p.Arg2063Trp)	rs781180388	0.00006
NM_001081.4(CUBN):c.7976T>C (p.Val2659Ala)	rs1007248288	0.00004
NM_001081.4(CUBN):c.8701G>A (p.Val2901Ile)	rs201093611	0.00004
NM_001081.4(CUBN):c.5851A>G (p.Ile1951Val)	rs1379361226	0.00001
NM_001081.4(CUBN):c.6847C>T (p.Arg2283Trp)	rs150117913	0.00001
NM_001081.4(CUBN):c.10250A>G (p.Asn3417Ser)
NM_001081.4(CUBN):c.18A>T (p.Leu6Phe)
NM_001081.4(CUBN):c.2845C>T (p.Pro949Ser)
NM_001081.4(CUBN):c.5840C>A (p.Ser1947Tyr)	rs147617753
NM_001081.4(CUBN):c.6772C>T (p.Arg2258Cys)
NM_001081.4(CUBN):c.9797G>C (p.Gly3266Ala)

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