Variant #0000834713 (NC_000002.11:g.21260934G>A, NM_000384.2:c.433C>T (APOB))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.21260934G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID APOB_000468 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs6752026
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0092 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-01-26 11:24:01 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOB NM_000384.2 -?/. - c.433C>T r.(?) p.(Pro145Ser)


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