Variant #0000001025 (NC_000002.12:g.21006167C>A, NM_000384.2:c.10701G>T (APOB))

Individual ID 00000201
Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.21006167C>A
Published as Thr3567Thr
Reference dbSNP, ClinVar
DB-ID APOB_000013
dbSNP ID rs12713558
Frequency 1/9
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
Date created 2020-11-30 12:43:29 +08:00 (CST)
Date last edited 2021-08-25 09:36:33 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
APOB NM_000384.2 -?/. 26 c.10701G>T - r.(=) p.(=) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000216 DNA DHPLC;SEQ APOB 9 Nuur Athirah Binti Mohd Daud