TNFRSF10A-DT TNFRSF10A divergent transcript

Information
Symbol
TNFRSF10A-DT
Type
ncRNA
Description
TNFRSF10A divergent transcript
Entrez Gene ID
389641
Genome
hg19
Position
chr8:23,082,734-23,088,439
Genome
hg38
Position
chr8:23,225,221-23,230,926
HGNC
HGNC:52647 HGNC
Ensembl
ENSG00000246582 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
SYNONYM PLACT1
HGNC HGNC:52647 HGNC
Ensembl ENSG00000246582 Ensembl
AllianceGenome HGNC:52647
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000500853.1 hg38 chr8 23,225,221 23,230,926 5,706
ENST00000670072.1 hg38 chr8 23,225,479 23,228,659 3,181
ENST00000500853.1 hg19 chr8 23,082,734 23,088,439 5,706
ENST00000670072.1 hg19 chr8 23,082,992 23,086,172 3,181
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