Variant #0000895037 (NC_000019.9:g.45411110T>C, NM_000041.2:c.137T>C (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.45411110T>C
DNA change (hg38) -
Published as APOE(NM_000041.4):c.137T>C (p.L46P), APOE(NM_001302688.2):c.215T>C (p.L72P)
ISCN -
DB-ID APOE_000011 See all 3 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) 0.00256 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
APOE NM_000041.2 -?/. - c.137T>C r.(?) p.(Leu46Pro) -
TOMM40 NM_001128916.1 -?/. - c.*4684T>C r.(=) p.(=) -


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