Variant #0000862296 (NC_000011.9:g.116661294_116661295dup, NM_001166598.1:c.653_654dup (APOA5))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.116661294_116661295dup
DNA change (hg38) -
Published as APOA5(NM_052968.5):c.653_654dupCC (p.A219Pfs*79)
ISCN -
DB-ID APOA5_000090
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 2022-05-09 15:51:19 +02:00 (CEST)
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     
APOA5 NM_001166598.1 +?/. - c.653_654dup r.(?) p.(Ala219Profs*79)
ZNF259 NM_003904.3 +?/. - c.-2586_-2585dup r.(?) p.(=)


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