Variant #0000518615 (NC_000003.11:g.184033616dup, NM_182917.4:c.32dup (EIF4G1))

Chromosome 3
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.184033616dup
DNA change (hg38) g.184315828dup
Published as EIF4G1(NM_001194946.1):c.32dup (p.(Pro12ThrfsTer50)), EIF4G1(NM_182917.4):c.32dupC (p.P12Tfs*43)
ISCN -
DB-ID EIF4G1_000060 See all 2 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF4G1 NM_182917.4 -?/. - c.32dup r.(?) p.(Pro12ThrfsTer43)


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