Variant #0000949586 (NC_000011.9:g.116707838dup, NM_000040.1:c.*4238dup (APOC3))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.116707838dup
DNA change (hg38) -
Published as APOA1(NM_001318017.1):c.85dupC (p.Q29Pfs*30), APOA1(NM_001318017.2):c.85dupC (p.Q29Pfs*30)
ISCN -
DB-ID APOA1_000066 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOA1 NM_000039.1 +/. - c.85dup r.(?) p.(Gln29ProfsTer30)
APOC3 NM_000040.1 +/. - c.*4238dup r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.