Variant #0000972065 (NC_000011.9:g.8016038C>T, NM_003754.2:c.719C>T (EIF3F))

Chromosome 11
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.8016038C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID EIF3F_000003
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs145163086
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00015 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-03-29 08:49:02 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF3F NM_003754.2 ?/. - c.719C>T r.(?) p.(Ala240Val)


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