Variant #0000889606 (NC_000011.9:g.116706564_116706587dup, NM_000040.1:c.*2964_*2987dup (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.116706564_116706587dup
DNA change (hg38) -
Published as APOA1(NM_001318021.1):c.414_437dupGAGCTTCAAGGTCAGCTTCCTGAG (p.L145_S146ins8)
ISCN -
DB-ID APOA1_000115
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 2022-11-01 13:01:21 +01:00 (CET)
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.741_764dup r.(?) p.(Leu254_Ser255insArgSerPheLysValSerPheLeu)
APOC3 NM_000040.1 ?/. - c.*2964_*2987dup r.(=) p.(=)


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