Variant #0001063373 (NC_000002.11:g.27591885_27591893del, NM_144631.5:c.*8519_*8527del (ZNF513))

Chromosome 2
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.27591885_27591893del
DNA change (hg38) -
Published as EIF2B4(NM_001034116.2):c.398_406del (p.(Thr133_Glu136delinsLys))
ISCN -
DB-ID EIF2B4_000036
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) 0.00018 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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF2B4 NM_001034116.1 ?/. - c.398_406del r.(?) p.(Thr133_Glu136delinsLys)
SNX17 NM_014748.3 ?/. - c.-1726_-1718del r.(?) p.(=)
ZNF513 NM_144631.5 ?/. - c.*8519_*8527del r.(=) p.(=)


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