Variant #0001025488 (NC_000008.10:g.144662832_144662840del, NM_032378.4:c.1554_1562del (EEF1D))

Chromosome 8
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.144662832_144662840del
DNA change (hg38) -
Published as EEF1D(NM_032378.7):c.1554_1562delCGAGGATGA (p.E519_D521del)
ISCN -
DB-ID EEF1D_000005
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EEF1D NM_032378.4 ?/. - c.1554_1562del r.(?) p.(Glu519_Asp521del)
NAPRT1 NM_145201.4 ?/. - c.-2344_-2336del r.(?) p.(=)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.