Variant #0001036770 (NC_000008.10:g.144658630G>A, NM_032378.4:c.*3332C>T (EEF1D))

Chromosome 8
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.144658630G>A
DNA change (hg38) -
Published as NAPRT(NM_145201.6):c.994C>T (p.(Arg332Cys))
ISCN -
DB-ID EEF1D_000006
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) 0.0048 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MROH6 NM_001100878.1 -?/. - c.-3746C>T r.(?) p.(=)
EEF1D NM_032378.4 -?/. - c.*3332C>T r.(=) p.(=)
NAPRT1 NM_145201.4 -?/. - c.994C>T r.(?) p.(Arg332Cys)


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