Variant #0000067102 (NC_000017.10:g.42956919C>T, NC_000017.10(NM_004247.3):c.702+5G>A (EFTUD2))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.42956919C>T
DNA change (hg38) g.44879551C>T
Published as -
ISCN -
DB-ID EFTUD2_000058 See all 2 reported entries
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 18:00:12 +02:00 (CEST)
Date last edited 2020-07-13 17:02:50 +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.702+5G>A r.(spl?) p.?


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