Variant #0001068172 (NC_000007.13:g.2400416A>G, NM_001037283.1:c.571A>G (EIF3B))

Chromosome 7
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.2400416A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID EIF3B_000016
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1779684995
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-02-09 14:54:02 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF3B NM_001037283.1 ?/. - c.571A>G r.(?) p.(Asn191Asp)


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