Variant #0000268787 (NC_000003.11:g.184039785_184039793del, NM_182917.4:c.1413_1421del (EIF4G1))

Chromosome 3
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.184039785_184039793del
DNA change (hg38) g.184321997_184322005del
Published as EIF4G1(NM_001194946.1):c.1434_1442delAGGAGAAGC (p.G479_A481del), EIF4G1(NM_182917.4):c.1413_1421delAGGAGAAGC (p.G472_A474del)
ISCN -
DB-ID EIF4G1_000016
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 14:54:23 +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.1413_1421del r.(?) p.(Gly472_Ala474del)


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