Variant #0000515546 (NC_000002.11:g.27592744C>A, NM_144631.5:c.*7668G>T (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.27592744C>A
DNA change (hg38) g.27369877C>A
Published as EIF2B4(NM_001034116.2):c.74G>T (p.(Gly25Val)), EIF2B4(NM_001318966.1):c.29G>T (p.G10V)
ISCN -
DB-ID EIF2B4_000019 See all 2 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF2B4 NM_001034116.1 ?/. - c.74G>T r.(?) p.(Gly25Val)
SNX17 NM_014748.3 ?/. - c.-867C>A r.(?) p.(=)
ZNF513 NM_144631.5 ?/. - c.*7668G>T r.(=) p.(=)


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