Variant #0000542395 (NC_000011.9:g.116661658_116661660del, NM_001166598.1:c.287_289del (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.116661658_116661660del
DNA change (hg38) g.116790942_116790944del
Published as APOA5(NM_052968.5):c.287_289delTGC (p.L96del)
ISCN -
DB-ID APOA5_000048
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 2019-07-18 18:22:55 +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.287_289del r.(?) p.(Leu96del)
ZNF259 NM_003904.3 +?/. - c.-2952_-2950del r.(?) p.(=)


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