Variant #0000067098 (NC_000017.10:g.42964016C>A, NM_004247.3:c.208G>T (EFTUD2))

Chromosome 17
Allele Unknown
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.42964016C>A
DNA change (hg38) g.44886648C>A
Published as -
ISCN -
DB-ID EFTUD2_000054
Variant remarks -
Reference Huang et al. 2015
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
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 17:37:46 +02:00 (CEST)
Date last edited 2020-07-13 17:03:00 +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 +/+ 3 c.208G>T r.(?) p.Glu70*


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