Genomic variant #0000274634

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.119708447C>T
DNA change (hg38) g.120574592C>T
Published as CUL4B(NM_003588.3):c.26G>A (p.G9E, p.(Gly9Glu))
ISCN -
DB-ID CUL4B_000048 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.00038 View details
Owner VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CUL4B NM_003588.3 -?/. - c.26G>A r.(?) p.(Gly9Glu)