Variant #0000676736 (NC_000002.11:g.88874891C>A, NM_004836.5:c.2110G>T (EIF2AK3))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.88874891C>A
DNA change (hg38) -
Published as EIF2AK3(NM_004836.6):c.2110G>T (p.A704S), EIF2AK3(NM_004836.7):c.2110G>T (p.A704S)
ISCN -
DB-ID EIF2AK3_000006 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) 0.69689 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.2110G>T r.(?) p.(Ala704Ser)


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