Variant #0000977110 (NC_000006.11:g.170871103del, NM_001172085.1:c.219del (TBP))

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.170871103del
DNA change (hg38) -
Published as TBP(NM_003194.5):c.279del (p.(Gln93HisfsTer51))
ISCN -
DB-ID TBP_000047
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 2024-04-19 20:27:30 +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     
TBP NM_001172085.1 ?/. - c.219del r.(?) p.(Gln73Hisfs*51)
TBP NM_003194.4 ?/. - c.279del r.(?) p.(Gln93Hisfs*51)


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