Variant #0001043517 (NC_000020.10:g.62124171_62124172insGGGA, NC_000020.10(NM_001958.3):c.772+321_772+322insCTCC (EEF1A2))

Chromosome 20
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.62124171_62124172insGGGA
DNA change (hg38) -
Published as EEF1A2(NM_001958.5):c.772+321_772+322insCTCC
ISCN -
DB-ID EEF1A2_000041
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_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     
EEF1A2 NM_001958.3 ?/. - c.772+321_772+322insCTCC r.(=) p.(=)


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