Variant #0000257968 (NC_000011.9:g.116706801_116706812del, NM_000040.1:c.*3201_*3212del (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.116706801_116706812del
DNA change (hg38) g.116836085_116836096del
Published as APOA1(NM_001318021.1):c.194_205delACCGCGCGCGCG (p.D65_R68del)
ISCN -
DB-ID APOA1_000004
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 2023-07-07 10:10:56 +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.521_532del r.(?) p.(Asp174_Arg177del)
APOC3 NM_000040.1 +/. - c.*3201_*3212del r.(=) p.(=)


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