Variant #0000727416 (NC_000019.9:g.45411063C>G, NM_000041.2:c.90C>G (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.45411063C>G
DNA change (hg38) -
Published as APOE(NM_001302688.2):c.168C>G (p.P56=)
ISCN -
DB-ID APOE_000036 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) 0.00012 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +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.90C>G r.(?) p.(Pro30=) -
TOMM40 NM_001128916.1 -?/. - c.*4637C>G r.(=) p.(=) -


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