List of variants in gene CUL3 reported as uncertain significance for CUL3-related disorder

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_003590.5(CUL3):c.67-11915T>C	rs1024746147	0.00002
NM_003590.5(CUL3):c.1720G>C (p.Glu574Gln)	rs1692154622	0.00001
NM_003590.5(CUL3):c.1289G>A (p.Arg430His)	rs2106197089
NM_003590.5(CUL3):c.1340C>T (p.Ser447Phe)	rs2106196731
NM_003590.5(CUL3):c.1376A>C (p.Lys459Thr)
NM_003590.5(CUL3):c.1547A>C (p.Gln516Pro)

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