Variant #0000271108 (NC_000005.9:g.176072256G>C, NC_000005.9(NM_001099408.1):c.474+12G>C (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.176072256G>C
DNA change (hg38) g.176645255G>C
Published as EIF4E1B(NM_001099408.2):c.474+12G>C
ISCN -
DB-ID EIF4E1B_000003
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) 0.00215 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 2018-01-15 20:58:59 +01:00 (CET)
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     
TSPAN17 NM_001006616.2 -?/. - c.-2361G>C r.(?) p.(=)
EIF4E1B NM_001099408.1 -?/. - c.474+12G>C r.(=) p.(=)


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