Variant #0000528686 (NC_000006.11:g.33281153del, NM_003190.4:c.312del (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.33281153del
DNA change (hg38) g.33313376del
Published as TAPBP(NM_003190.4):c.312delA (p.K104Nfs*6)
ISCN -
DB-ID TAPBP_000007
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-19 11:20:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZBTB22 NM_001145338.1 ?/. - c.*1638del r.(?) p.(=)
TAPBP NM_003190.4 ?/. - c.312del r.(?) p.(Lys104AsnfsTer6)


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