Variant #0000542466 (NC_000011.9:g.116707838dup, NM_000040.1:c.*4238dup (APOC3))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.116707838dup
DNA change (hg38) g.116837122dup
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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.(=)


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