Variant #0000676609 (NC_000002.11:g.27592755G>A, NM_144631.5:c.*7657C>T (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.27592755G>A
DNA change (hg38) -
Published as EIF2B4(NM_001318966.1):c.18C>T (p.P6=)
ISCN -
DB-ID EIF2B4_000022
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF2B4 NM_001034116.1 -?/. - c.63C>T r.(?) p.(Pro21=)
SNX17 NM_014748.3 -?/. - c.-856G>A r.(?) p.(=)
ZNF513 NM_144631.5 -?/. - c.*7657C>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.