Variant #0001033254 (NC_000002.11:g.27589688C>G, NM_144631.5:c.*10724G>C (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.27589688C>G
DNA change (hg38) -
Published as EIF2B4(NM_001034116.2):c.1129G>C (p.(Val377Leu))
ISCN -
DB-ID EIF2B4_000032
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) 1.0E-5 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     
EIF2B4 NM_001034116.1 ?/. - c.1129G>C r.(?) p.(Val377Leu)
SNX17 NM_014748.3 ?/. - c.-3923C>G r.(?) p.(=)
ZNF513 NM_144631.5 ?/. - c.*10724G>C r.(=) p.(=)


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