Genomic variant #0000579874

Individual ID 00249531
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.21260829C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID APOB_000170 See all 3 reported entries
Variant remarks normal 2nd chromosome
Reference PubMed: Leren 2008
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 LOVD




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
APOB NM_000384.2 +/+? 5i c.537+1G>T pathogenic r.(?) p.(?)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000250638 DNA SEQ - - APOB 1 -