Variant #0000677692 (NC_000006.11:g.170871100_170871105dup, NM_001172085.1:c.216_221dup (TBP))

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.170871100_170871105dup
DNA change (hg38) -
Published as TBP(NM_003194.5):c.276_281dupGCAGCA (p.Q94_Q95dup)
ISCN -
DB-ID TBP_000040
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
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBP NM_001172085.1 -/. - c.216_221dup r.(?) p.(Gln74_Gln75dup)
TBP NM_003194.4 -/. - c.276_281dup r.(?) p.(Gln94_Gln95dup)


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