Genomic variant #0000018566

Individual ID 00001418
Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.153784412del
DNA change (hg38) -
Published as -
ISCN -
DB-ID IKBKG_000011
Variant remarks -
Reference PubMed: Aradhya et al.2001
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 Francesca Fusco




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
IKBKG NM_003639.3 ?/? 3 c.220del - r.(?) p.(Glu74Serfs*41)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000001188 DNA ? - - IKBKG 1 Francesca Fusco