Variant #0000528033 (NC_000006.11:g.170871040_170871041insG, TBP(NM_001172085.1):c.156_157insG)

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.170871040_170871041insG
DNA change (hg38) g.170561952_170561953insG
Published as TBP(NM_003194.4):c.216_217insG (p.Q73Afs*105)
ISCN -
DB-ID TBP_000023
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBP NM_001172085.1 -/. - c.156_157insG r.(?) p.(Gln53AlafsTer105)
TBP NM_003194.4 -/. - c.216_217insG r.(?) p.(Gln73AlafsTer105)