Genomic variant #0000439832

Individual ID 00208600
Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43166414_43166416del
DNA change (hg38) -
Published as -
ISCN -
DB-ID CUL9_000004
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs141674093
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Xiang Jiao




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
CUL9 NM_015089.2 ?/. - c.2871_2873del - r.(?) p.(Gly958del)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000209649 DNA SEQ-NG-I Blood - - 12 Xiang Jiao