List of variants in gene CUL4B reported as uncertain significance for Inborn genetic diseases

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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_003588.4(CUL4B):c.67+10T>C	rs992197854	0.00011
NM_001079872.2(CUL4B):c.1309G>A (p.Ala437Thr)	rs757649304	0.00002
NM_001079872.2(CUL4B):c.1257-10T>C	rs1924093632
NM_001079872.2(CUL4B):c.1325-3C>T	rs1569390239
NM_001079872.2(CUL4B):c.1397G>C (p.Arg466Pro)	rs1172227126
NM_001079872.2(CUL4B):c.1443+3A>G	rs1923999235
NM_001079872.2(CUL4B):c.2041C>A (p.Pro681Thr)	rs1556196865
NM_001079872.2(CUL4B):c.709A>G (p.Asn237Asp)
NM_001079872.2(CUL4B):c.902C>T (p.Ser301Leu)	rs1924258472
NM_001079872.2(CUL4B):c.916A>C (p.Ile306Leu)

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