Variant #0000911681 (NC_000002.11:g.27589810T>C, NM_144631.5:c.*10602A>G (ZNF513))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27589810T>C
DNA change (hg38) -
Published as EIF2B4(NM_001034116.2):c.1014-7A>G, EIF2B4(NM_001318966.2):c.969-7A>G
ISCN -
DB-ID EIF2B4_000013 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) 0.40084 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-01-11 15:44:22 +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.1014-7A>G r.(=) p.(=)
SNX17 NM_014748.3 -/. - c.-3801T>C r.(?) p.(=)
ZNF513 NM_144631.5 -/. - c.*10602A>G r.(=) p.(=)


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