Variant #0000314439 (NC_000006.11:g.170871052_170871053del, TBP(NM_001172085.1):c.168_169del)

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.170871052_170871053del
DNA change (hg38) g.170561964_170561965del
Published as TBP(NM_003194.5):c.228_229delGC (p.Q77Afs*100)
ISCN -
DB-ID TBP_000010
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBP NM_001172085.1 -?/. - c.168_169del r.(?) p.(Gln57AlafsTer100)
TBP NM_003194.4 -?/. - c.228_229del r.(?) p.(Gln77AlafsTer100)