Variant #0000542400 (NC_000011.9:g.116662297C>G, NC_000011.9(NM_001166598.1):c.161+5G>C (APOA5))

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.116662297C>G
DNA change (hg38) g.116791581C>G
Published as APOA5(NM_052968.5):c.161+5G>C
ISCN -
DB-ID APOA5_000053
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) 3.0E-5 View details
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.161+5G>C r.spl? p.?
ZNF259 NM_003904.3 +/. - c.-3591G>C r.(?) p.(=)


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