Variant #0000528689 (NC_000006.11:g.33281505C>A, NM_003190.4:c.174G>T (TAPBP))

Chromosome 6
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.33281505C>A
DNA change (hg38) g.33313728C>A
Published as TAPBP(NM_003190.4):c.174G>T (p.P58=)
ISCN -
DB-ID DAXX_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) 0.00508 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-19 11:21:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DAXX NM_001141970.1 -?/. - c.*5015G>T r.(=) p.(=)
ZBTB22 NM_001145338.1 -?/. - c.*1284G>T r.(=) p.(=)
TAPBP NM_003190.4 -?/. - c.174G>T r.(?) p.(Pro58=)


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