TDRD12 tudor domain containing 12

Information
Symbol
TDRD12
Type
protein-coding
Description
tudor domain containing 12
Entrez Gene ID
91646
Genome
hg19
Position
chr19:33,210,673-33,320,486
Genome
hg38
Position
chr19:32,719,767-32,829,580
HGNC
HGNC:25044 HGNC
Ensembl
ENSG00000173809 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 8
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 48
Ranking
ClinVar
0
0
2
56
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
Category :
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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 :
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 ECAT8
HGNC HGNC:25044 HGNC
Ensembl ENSG00000173809 Ensembl
AllianceGenome HGNC:25044
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000639142.2 hg38 chr19 32,719,767 32,829,580 109,814
ENST00000444215.6 hg38 chr19 32,719,753 32,821,263 101,511
ENST00000647536.1 hg38 chr19 32,720,013 32,827,414 107,402
ENST00000421545.2 hg38 chr19 32,720,073 32,790,808 70,736
ENST00000444215.6 hg19 chr19 33,210,659 33,312,169 101,511
ENST00000639142.2 hg19 chr19 33,210,673 33,320,486 109,814
ENST00000647536.1 hg19 chr19 33,210,919 33,318,320 107,402
ENST00000421545.2 hg19 chr19 33,210,979 33,281,714 70,736
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