Variant #0000983522 (NC_000019.9:g.45411858C>G, NM_000041.2:c.305C>G (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.45411858C>G
DNA change (hg38) -
Published as APOE(NM_000041.4):c.305C>G (p.(Pro102Arg)), APOE(NM_001302688.2):c.383C>G (p.P128R)
ISCN -
DB-ID APOE_000085 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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.305C>G r.(?) p.(Pro102Arg) -
TOMM40 NM_001128916.1 ?/. - c.*5432C>G r.(=) p.(=) -


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