Genomic variant #0000038988

Individual ID 00018538
Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.76788942_76788950delinsAAAAACCAAAA
DNA change (hg38) g.75029184_75029192delinsAAAAACCAAAA
Published as -
ISCN -
DB-ID KAT6B_000003
Variant remarks -
Reference PubMed: Campeau et al.
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 Philippe Campeau




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
KAT6B NM_012330.3 +/+ 18 c.4360_4368delinsAAAAACCAAAA - r.(?) p.(Glu1454Lysfs*8)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000018522 DNA SEQ - - KAT6B 1 Philippe Campeau