TBCB tubulin folding cofactor B

Information
Symbol
TBCB
Type
protein-coding
Description
tubulin folding cofactor B
Entrez Gene ID
1155
Genome
hg19
Position
chr19:36,606,370-36,616,843
Genome
hg38
Position
chr19:36,115,468-36,125,941
MIM
601303 OMIM
HGNC
HGNC:1989 HGNC
Ensembl
ENSG00000105254 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 42
Ranking
ClinVar
0
0
0
42
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
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Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
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Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM CG22
SYNONYM CKAP1
SYNONYM CKAPI
MIM 601303 OMIM
HGNC HGNC:1989 HGNC
Ensembl ENSG00000105254 Ensembl
AllianceGenome HGNC:1989
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000586868.1 hg38 chr19 36,116,072 36,125,947 9,876
ENST00000585746.1 hg38 chr19 36,115,838 36,125,945 10,108
ENST00000651435.1 hg38 chr19 36,115,506 36,125,945 10,440
ENST00000589996.5 hg38 chr19 36,115,519 36,125,778 10,260
ENST00000629269.2 hg38 chr19 36,115,439 36,118,560 3,122
ENST00000221855.8 hg38 chr19 36,115,468 36,125,941 10,474
ENST00000629269.2 hg19 chr19 36,606,341 36,609,462 3,122
ENST00000221855.8 hg19 chr19 36,606,370 36,616,843 10,474
ENST00000651435.1 hg19 chr19 36,606,408 36,616,847 10,440
ENST00000589996.5 hg19 chr19 36,606,421 36,616,680 10,260
ENST00000585746.1 hg19 chr19 36,606,740 36,616,847 10,108
ENST00000586868.1 hg19 chr19 36,606,974 36,616,849 9,876
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