TCF20 transcription factor 20

Information
Symbol
TCF20
Type
protein-coding
Description
transcription factor 20
Entrez Gene ID
6942
Genome
hg19
Position
chr22:42,556,059-42,665,622
Genome
hg38
Position
chr22:42,160,053-42,269,616
MIM
603107 OMIM
HGNC
HGNC:11631 HGNC
Ensembl
ENSG00000100207 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 154
Likely pathogenic 0 34
Benign 0 148
Likely benign 0 526
Conflicting classifications of pathogenicity 0 54
Uncertain significance 0 744
Ranking
ClinVar
0
0
204
1,334
30
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
Category :
Search word :
Filtering :
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 :
Search word :
Filtering :
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 AR1
SYNONYM DDVIBA
SYNONYM SPBP
SYNONYM TCF-20
MIM 603107 OMIM
HGNC HGNC:11631 HGNC
Ensembl ENSG00000100207 Ensembl
AllianceGenome HGNC:11631
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000404876.1 hg38 chr22 42,161,098 42,210,208 49,111
ENST00000335626.8 hg38 chr22 42,161,056 42,215,440 54,385
ENST00000359486.8 hg38 chr22 42,160,013 42,283,997 123,985
ENST00000677622.1 hg38 chr22 42,160,013 42,270,653 110,641
ENST00000683686.1 hg38 chr22 42,160,053 42,269,616 109,564
ENST00000677622.1 hg19 chr22 42,556,019 42,666,659 110,641
ENST00000359486.8 hg19 chr22 42,556,019 42,680,003 123,985
ENST00000683686.1 hg19 chr22 42,556,059 42,665,622 109,564
ENST00000335626.8 hg19 chr22 42,557,062 42,611,446 54,385
ENST00000404876.1 hg19 chr22 42,557,104 42,606,214 49,111
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