Variant #0001015804 (NC_000019.9:g.45451799G>C, NC_000019.9(NM_000483.4):c.55+9G>C (APOC2))

Chromosome 19
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.45451799G>C
DNA change (hg38) -
Published as APOC2(NM_000483.5):c.55+9G>C
ISCN -
DB-ID APOC2_000064
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 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOC2 NM_000483.4 -?/. - c.55+9G>C r.(=) p.(=)
APOC4 NM_001646.2 -?/. - c.*3237G>C r.(=) p.(=)
APOC4-APOC2 NR_037932.1 -?/. - n.1262+9G>C r.(?) -


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