Variant #0000624004 (NC_000019.9:g.4054526_4054532dup, NM_015898.2:c.699_705dup (ZBTB7A))

Chromosome 19
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.4054526_4054532dup
DNA change (hg38) g.4054528_4054534dup
Published as ZBTB7A(NM_015898.4):c.699_705dupCGGGGAC (p.E236Rfs*16)
ISCN -
DB-ID ZBTB7A_000002
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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-07-15 10:08:29 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZBTB7A NM_015898.2 ?/. - c.699_705dup r.(?) p.(Glu236ArgfsTer16)


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