Variant #0001071780 (NC_000023.10:g.24073742A>G, NM_001415.3:c.80A>G (EIF2S3))

Chromosome X
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.24073742A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID EIF2S3_000033
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs776243738
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-01 16:33:02 +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     
EIF2S3 NM_001415.3 -?/. - c.80A>G r.(?) p.(Lys27Arg)


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