Variant #0000268799 (NC_000003.11:g.184049385C>T, NM_182917.4:c.4389C>T (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.184049385C>T
DNA change (hg38) g.184331597C>T
Published as EIF4G1(NM_001194946.1):c.4407C>T (p.D1469=), EIF4G1(NM_182917.4):c.4389C>T (p.D1463=)
ISCN -
DB-ID EIF4G1_000049 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) 0.01228 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-16 09:24:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN2 NM_004366.5 -/. - c.*15009G>A r.(=) p.(=)
FAM131A NM_144635.4 -/. - c.-6034C>T r.(?) p.(=)
EIF4G1 NM_182917.4 -/. - c.4389C>T r.(?) p.(Asp1463=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.