Variant #0000257998 (NC_000011.9:g.116662569C>T, NM_001166598.1:c.8G>A (APOA5))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.116662569C>T
DNA change (hg38) g.116791853C>T
Published as APOA5(NM_052968.5):c.8G>A (p.S3N)
ISCN -
DB-ID APOA5_000030
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 2023-01-11 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.8G>A r.(?) p.(Ser3Asn)
ZNF259 NM_003904.3 -?/. - c.-3863G>A r.(?) p.(=)


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