Variant #0000528057 (NC_000006.11:g.170873705C>T, TBP(NM_001172085.1):c.510C>T)

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.170873705C>T
DNA change (hg38) g.170564617C>T
Published as TBP(NM_003194.4):c.570C>T (p.A190=)
ISCN -
DB-ID TBP_000034
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) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBP NM_001172085.1 -?/. - c.510C>T r.(?) p.(Ala170=)
TBP NM_003194.4 -?/. - c.570C>T r.(?) p.(Ala190=)