Variant #0000723204 (NC_000011.9:g.116703570G>A, NM_000040.1:c.270G>A (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.116703570G>A
DNA change (hg38) -
Published as APOC3(NM_000040.3):c.270G>A (p.E90=)
ISCN -
DB-ID APOA1_000092
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) 1.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOA1 NM_000039.1 ?/. - c.*2954C>T r.(=) p.(=)
APOC3 NM_000040.1 ?/. - c.270G>A r.(?) p.(Glu90=)


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