Variant #0000692825 (NC_000019.9:g.45409433dup, NC_000019.9(NM_000041.2):c.-24+335dup (APOE))

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.45409433dup
DNA change (hg38) -
Published as APOE(NM_001302688.2):c.55+253dupA
ISCN -
DB-ID APOE_000079
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 2020-09-15 15:50:26 +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     

Haplotype     
APOE NM_000041.2 -?/. - c.-24+335dup r.(=) p.(=) -
TOMM40 NM_001128916.1 -?/. - c.*3007dup r.(?) p.(=) -


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