Variant #0000525243 (NC_000005.9:g.176056539G>A, NM_001099408.1:c.-1728G>A (EIF4E1B))

Chromosome 5
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.176056539G>A
DNA change (hg38) g.176629538G>A
Published as SNCB(NM_001001502.3):c.117C>T (p.Y39=)
ISCN -
DB-ID EIF4E1B_000004
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SNCB NM_001001502.1 -?/. - c.117C>T r.(?) p.(Tyr39=)
EIF4E1B NM_001099408.1 -?/. - c.-1728G>A r.(?) p.(=)


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