Variant #0000802448 (NC_000006.11:g.170871055_170871067del, TBP(NM_001172085.1):c.171_183del)

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.170871055_170871067del
DNA change (hg38) -
Published as TBP(NM_003194.4):c.231_243delGCAGCAGCAGCAG (p.Q77Hfs*63), TBP(NM_003194.5):c.231_243delGCAGCAGCAGCAG (p.Q77Hfs*63)
ISCN -
DB-ID TBP_000014 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBP NM_001172085.1 -?/. - c.171_183del r.(?) p.(Gln57HisfsTer63)
TBP NM_003194.4 -?/. - c.231_243del r.(?) p.(Gln77HisfsTer63)