Variant #0000720809 (NC_000006.11:g.170871176G>A, TBP(NM_001172085.1):c.292G>A)

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.170871176G>A
DNA change (hg38) -
Published as TBP(NM_003194.4):c.352G>A (p.A118T)
ISCN -
DB-ID TBP_000042
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) 0.0002 View details
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.292G>A r.(?) p.(Ala98Thr)
TBP NM_003194.4 -?/. - c.352G>A r.(?) p.(Ala118Thr)