Variant #0000067101 (NC_000017.10:g.42960460C>T, NC_000017.10(NM_004247.3):c.492+1G>A (EFTUD2))

Chromosome 17
Allele Maternal (confirmed)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.42960460C>T
DNA change (hg38) g.44883092C>T
Published as -
ISCN -
DB-ID EFTUD2_000057
Variant remarks -
Reference Huang et al. 2015
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Dennis E. Bulman
Database submission license No license selected
Created by Dennis E. Bulman
Date created 2015-06-09 17:45:10 +02:00 (CEST)
Date last edited 2020-07-13 17:02:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EFTUD2 NM_004247.3 +/+ - c.492+1G>A r.spl? p.?


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