Variant #0000689685 (NC_000006.11:g.170871055_170871082del, NM_001172085.1:c.171_198del (TBP))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.170871055_170871082del
DNA change (hg38) -
Published as TBP(NM_003194.4):c.231_258delGCAGCAGCAGCAGCAGCAGCAGCAGCAG (p.Q77Hfs*58), TBP(NM_003194.5):c.231_258del (p.(Gln77HisfsTer58))
ISCN -
DB-ID TBP_000041 See all 2 reported entries
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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBP NM_001172085.1 -/. - c.171_198del r.(?) p.(Gln57HisfsTer58)
TBP NM_003194.4 -/. - c.231_258del r.(?) p.(Gln77HisfsTer58)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.