Variant #0000631894 (NC_000002.11:g.88879079C>A, NM_004836.5:c.1843G>T (EIF2AK3))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.88879079C>A
DNA change (hg38) g.88579561C>A
Published as [1843G>T];[1844A>C]
ISCN -
DB-ID EIF2AK3_000040
Variant remarks correct is two flanking variants on one allele (c.1843_1844inv)
Reference Journal: Wakeling 2020
ClinVar ID -
dbSNP ID -
Origin Artefact
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-01-23 14:28:43 +01:00 (CET)
Date last edited 2020-07-14 22:03:31 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF2AK3 NM_004836.5 ?/. - c.1843G>T r.(?) p.(Asp615Tyr)


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