Variant #0000866168 (NC_000019.9:g.45449284T>G, NM_000483.4:c.-62T>G (APOC2))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45449284T>G
DNA change (hg38) -
Published as APOC2(NM_000483.4):c.-62T>G
ISCN -
DB-ID APOC2_000049
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOC2 NM_000483.4 -/. - c.-62T>G r.(?) p.(=)
APOC4 NM_001646.2 -/. - c.*722T>G r.(=) p.(=)
APOC4-APOC2 NR_037932.1 -/. - n.1146T>G r.(?) -


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