Variant #0000998753 (NC_000011.9:g.116707739A>C, NM_000040.1:c.*4139A>C (APOC3))

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.116707739A>C
DNA change (hg38) -
Published as APOA1(NM_000039.1):c.178T>G (p.(Ser60Ala)), APOA1(NM_000039.3):c.178T>G (p.S60A), APOA1(NM_001318017.2):c.178T>G (p.S60A)
ISCN -
DB-ID APOA1_000014 See all 2 reported entries
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) 0.00032 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
APOA1 NM_000039.1 -?/. - c.178T>G r.(?) p.(Ser60Ala)
APOC3 NM_000040.1 -?/. - c.*4139A>C r.(=) p.(=)


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