Variant #0000993478 (NC_000003.11:g.184049331C>G, NM_182917.4:c.4335C>G (EIF4G1))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.184049331C>G
DNA change (hg38) -
Published as EIF4G1(NM_198241.2):c.4332C>G (p.(Asn1444Lys))
ISCN -
DB-ID EIF4G1_000124
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN2 NM_004366.5 ?/. - c.*15063G>C r.(=) p.(=)
FAM131A NM_144635.4 ?/. - c.-6088C>G r.(?) p.(=)
EIF4G1 NM_182917.4 ?/. - c.4335C>G r.(?) p.(Asn1445Lys)


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