Variant #0000331354 (NC_000006.11:g.170873706G>C, TBP(NM_001172085.1):c.511G>C)

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.170873706G>C
DNA change (hg38) g.170564618G>C
Published as TBP(NM_001172085.1):c.511G>C (p.(Glu171Gln))
ISCN -
DB-ID TBP_000017
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBP NM_001172085.1 ?/. - c.511G>C r.(?) p.(Glu171Gln)
TBP NM_003194.4 ?/. - c.571G>C r.(?) p.(Glu191Gln)