Variant #0000001090 (NC_000002.12:g.21037264G>A, APOB(NM_000384.2):c.538-9C>T)

Individual ID 00000214
Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.21037264G>A
Published as -
Reference Livy Alex et al. (2012), dbSNP, ClinVar
DB-ID APOB_000031
dbSNP ID rs1800478
Frequency 1/17
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
APOB NM_000384.2 ./. 5i c.538-9C>T - r.(=) p.(=) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000229 DNA SEQ-NG-I APOB 17 Nuur Athirah Binti Mohd Daud