CT69 cancer/testis associated transcript 69

Information
Symbol
CT69
Type
ncRNA
Description
cancer/testis associated transcript 69
Entrez Gene ID
101928231
Genome
hg19
Position
chr6:134,749,377-134,796,638
Genome
hg38
Position
chr6:134,428,239-134,475,500
HGNC
HGNC:37196 HGNC
Ensembl
ENSG00000231971 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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 :
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
HGNC HGNC:37196 HGNC
Ensembl ENSG00000231971 Ensembl
AllianceGenome HGNC:37196
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000668601.1 hg38 chr6 134,436,526 134,476,554 40,029
ENST00000657570.1 hg38 chr6 134,428,239 134,475,500 47,262
ENST00000660051.1 hg38 chr6 134,428,243 134,476,565 48,323
ENST00000657570.1 hg19 chr6 134,749,377 134,796,638 47,262
ENST00000660051.1 hg19 chr6 134,749,381 134,797,703 48,323
ENST00000668601.1 hg19 chr6 134,757,664 134,797,692 40,029
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