Genomic variant #0000573307

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.119673192del
DNA change (hg38) -
Published as CUL4B(NM_001079872.1):c.1674del (p.(Glu559LysfsTer15), p.(Glu577LysfsTer15))
ISCN -
DB-ID CUL4B_000066
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
CUL4B NM_003588.3 +?/. - c.1728del likely pathogenic r.(?) p.(Glu577Lysfs*15)