Variant #0000998747 (NC_000011.9:g.116661750G>A, NM_001166598.1:c.195C>T (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.116661750G>A
DNA change (hg38) -
Published as APOA5(NM_052968.5):c.195C>T (p.N65=)
ISCN -
DB-ID APOA5_000125
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) 0.00022 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOA5 NM_001166598.1 -?/. - c.195C>T r.(?) p.(=)
ZNF259 NM_003904.3 -?/. - c.-3044C>T r.(?) p.(=)


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