Variant #0000542399 (NC_000011.9:g.116661789G>T, NC_000011.9(NM_001166598.1):c.162-6C>A (APOA5))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.116661789G>T
DNA change (hg38) g.116791073G>T
Published as APOA5(NM_052968.5):c.162-6C>A
ISCN -
DB-ID APOA5_000052
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.162-6C>A r.(=) p.(=)
ZNF259 NM_003904.3 ?/. - c.-3083C>A r.(?) p.(=)


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