Variant #0000915246 (NC_000019.9:g.45409180G>A, NC_000019.9(NM_000041.2):c.-24+82G>A (APOE))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.45409180G>A
DNA change (hg38) -
Published as APOE(NM_000041.4):c.-24+82G>A, APOE(NM_001302688.2):c.55G>A (p.D19N)
ISCN -
DB-ID APOE_000006 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) 0.00054 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +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     

Haplotype     
APOE NM_000041.2 ?/. - c.-24+82G>A r.(=) p.(=) -
TOMM40 NM_001128916.1 ?/. - c.*2754G>A r.(=) p.(=) -


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