Variant #0000726454 (NC_000017.10:g.42945648_42945652del, NC_000017.10(NM_004247.3):c.1058+3_1058+7del (EFTUD2))

Chromosome 17
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.42945648_42945652del
DNA change (hg38) -
Published as EFTUD2(NM_001142605.1):c.953+3_953+7del (p.?), EFTUD2(NM_001258353.1):c.1058+3_1058+7delAAGTA, EFTUD2(NM_001258353.2):c.1058+3_1058+7delAAGTA
ISCN -
DB-ID EFTUD2_000022 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00548 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +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.1058+3_1058+7del r.spl? p.?


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