Variant #0000851200 (NC_000006.11:g.33287819_33287821del, NM_001145338.1:c.-2234_-2232del (ZBTB22))

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.33287819_33287821del
DNA change (hg38) -
Published as DAXX(NM_001350.4):c.1434_1436delAGA (p.E480del)
ISCN -
DB-ID DAXX_000005
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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DAXX NM_001141970.1 ?/. - c.1470_1472del r.(?) p.(Glu492del)
ZBTB22 NM_001145338.1 ?/. - c.-2234_-2232del r.(?) p.(=)


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