Variant #0000802559 (NC_000006.11:g.33282893C>A, NM_003190.4:c.-1075G>T (TAPBP))

Chromosome 6
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.33282893C>A
DNA change (hg38) -
Published as ZBTB22(NM_001145338.1):c.1801G>T (p.(Asp601Tyr))
ISCN -
DB-ID DAXX_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
DAXX NM_001141970.1 ?/. - c.*3627G>T r.(=) p.(=)
ZBTB22 NM_001145338.1 ?/. - c.1801G>T r.(?) p.(Asp601Tyr)
TAPBP NM_003190.4 ?/. - c.-1075G>T r.(?) p.(=)


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