Variant #0000800563 (NC_000002.11:g.27591919T>C, NM_144631.5:c.*8493A>G (ZNF513))

Chromosome 2
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.27591919T>C
DNA change (hg38) -
Published as EIF2B4(NM_001318966.1):c.327A>G (p.G109=)
ISCN -
DB-ID EIF2B4_000025
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) 0.00059 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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.372A>G r.(?) p.(Gly124=)
SNX17 NM_014748.3 -?/. - c.-1692T>C r.(?) p.(=)
ZNF513 NM_144631.5 -?/. - c.*8493A>G r.(=) p.(=)


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