List of variants in gene CUL3 reported as uncertain significance by Ambry 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_003590.5(CUL3):c.1030-6T>C	rs368109133	0.00001
NM_003590.5(CUL3):c.1433G>C (p.Ser478Thr)	rs766416620	0.00001
NM_003590.5(CUL3):c.1849C>G (p.Gln617Glu)	rs969388164	0.00001
NM_003590.5(CUL3):c.2222T>C (p.Ile741Thr)	rs778175467	0.00001
NM_003590.5(CUL3):c.532G>A (p.Val178Ile)	rs1200173088	0.00001
NM_003590.5(CUL3):c.778A>G (p.Ile260Val)	rs748814630	0.00001
NM_003590.5(CUL3):c.1166C>T (p.Ser389Leu)	rs2106202854
NM_003590.5(CUL3):c.1590T>G (p.His530Gln)	rs1574631853
NM_003590.5(CUL3):c.1600A>G (p.Ile534Val)
NM_003590.5(CUL3):c.1808T>C (p.Met603Thr)	rs200435739
NM_003590.5(CUL3):c.1826A>G (p.Glu609Gly)	rs755967005
NM_003590.5(CUL3):c.1864A>G (p.Ile622Val)	rs2106152416
NM_003590.5(CUL3):c.2164C>G (p.Leu722Val)	rs1378177790
NM_003590.5(CUL3):c.2236G>C (p.Glu746Gln)
NM_003590.5(CUL3):c.265G>A (p.Val89Met)	rs1350012050
NM_003590.5(CUL3):c.540-5G>A	rs747752633

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