Variant #0000866171 (NC_000019.9:g.45452037_45452038del, NM_000483.4:c.135_136del (APOC2))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45452037_45452038del
DNA change (hg38) -
Published as APOC2(NM_000483.4):c.135_136delCA (p.S46Lfs*23)
ISCN -
DB-ID APOC2_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_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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOC2 NM_000483.4 +/. - c.135_136del r.(?) p.(Ser46Leufs*23)
APOC4 NM_001646.2 +/. - c.*3475_*3476del r.(=) p.(=)
APOC4-APOC2 NR_037932.1 +/. - n.1342_1343del r.(?) -


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