Variant #0000677691 (NC_000006.11:g.170871084A>G, TBP(NM_001172085.1):c.200A>G)

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.170871084A>G
DNA change (hg38) -
Published as TBP(NM_003194.4):c.260A>G (p.Q87R)
ISCN -
DB-ID TBP_000039
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.200A>G r.(?) p.(Gln67Arg)
TBP NM_003194.4 -?/. - c.260A>G r.(?) p.(Gln87Arg)