Variant #0000887124 (NC_000006.11:g.170871057_170871058insACAGCAACA, TBP(NM_001172085.1):c.173_174insACAGCAACA)

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.170871057_170871058insACAGCAACA
DNA change (hg38) -
Published as TBP(NM_003194.5):c.233_234insACAGCAACA (p.Q93_Q95dup)
ISCN -
DB-ID TBP_000045
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.173_174insACAGCAACA r.(?) p.(Gln73_Gln75dup)
TBP NM_003194.4 -?/. - c.233_234insACAGCAACA r.(?) p.(Gln93_Gln95dup)