Genomic variant #0000579885

Individual ID 00249473
Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.21256269_21256276del
DNA change (hg38) -
Published as -
ISCN -
DB-ID APOB_000070
Variant remarks apoB-6.9; normal 2nd chromosome
Reference PubMed: Whitfield 2003
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Amanda Hooper




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
APOB NM_000384.2 +/+? 9 c.1019_1026del pathogenic r.(?) p.(Gln340Profs*4)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000250580 DNA SEQ - - APOB 1 Amanda Hooper