Variant #0000862302 (NC_000011.9:g.116701535T>C, NM_000040.1:c.102T>C (APOC3))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.116701535T>C
DNA change (hg38) -
Published as APOC3(NM_000040.2):c.102T>C (p.G34=), APOC3(NM_000040.3):c.102T>C (p.G34=)
ISCN -
DB-ID APOC3_000006 See all 3 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) 0.64707 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOA1 NM_000039.1 -/. - c.*4989A>G r.(=) p.(=)
APOC3 NM_000040.1 -/. - c.102T>C r.(?) p.(Gly34=)


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