Variant #0000247051 (NC_000011.9:g.116706723A>G, NM_000040.1:c.*3123A>G (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.116706723A>G
DNA change (hg38) g.116836007A>G
Published as APOA1(NM_000039.3):c.605T>C (p.L202P), APOA1(NM_001318021.1):c.278T>C (p.L93P)
ISCN -
DB-ID APOA1_000013 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOA1 NM_000039.1 +/. - c.605T>C r.(?) p.(Leu202Pro)
APOC3 NM_000040.1 +/. - c.*3123A>G r.(=) p.(=)


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