Full data view for gene CUL4B

Information The variants shown are described using the NM_003588.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-?/. - c.194_202del r.(?) p.(Ser65_Ser67del) Unknown - likely benign g.119694356_119694364del - CUL4B(NM_001079872.1):c.140_148del (p.(Ser47_Ser49del)), CUL4B(NM_003588.3):c.194_202delGCAGCAGTA (p.S65_S67del) - CUL4B_000071 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.194_202del r.(?) p.(Ser65_Ser67del) Unknown - benign g.119694356_119694364del - CUL4B(NM_001079872.1):c.140_148del (p.(Ser47_Ser49del)), CUL4B(NM_003588.3):c.194_202delGCAGCAGTA (p.S65_S67del) - CUL4B_000071 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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