Genomic variant #0000036891

Individual ID 00017008
Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.119694117_119694119dup
DNA change (hg38) g.120560262_120560264dup
Published as -
ISCN -
DB-ID CUL4B_000010
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Andreas Tzschach




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
CUL4B NM_003588.3 +?/? 3 c.429_431dup - r.(?) p.(Ser146dup)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000016985 DNA SEQ - - CUL4B 1 Andreas Tzschach