Variant #0000617674 (NC_000019.9:g.45409917C>A, NM_000041.2:c.36C>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.45409917C>A
DNA change (hg38) g.44906660C>A
Published as APOE(NM_001302688.2):c.114C>A (p.F38L)
ISCN -
DB-ID APOE_000057
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) 1.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
APOE NM_000041.2 ?/. - c.36C>A r.(?) p.(Phe12Leu) -
TOMM40 NM_001128916.1 ?/. - c.*3491C>A r.(=) p.(=) -


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