PDGFA-DT PDGFA divergent transcript

Information
Symbol
PDGFA-DT
Type
ncRNA
Description
PDGFA divergent transcript
Entrez Gene ID
441307
Genome
hg19
Position
chr7:560,028-564,869
Genome
hg38
Position
chr7:520,391-525,232
HGNC
HGNC:55865 HGNC
Ensembl
ENSG00000223855 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 HRAT92
HGNC HGNC:55865 HGNC
Ensembl ENSG00000223855 Ensembl
AllianceGenome HGNC:55865
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000702988.1 hg38 chr7 522,596 525,233 2,638
ENST00000689546.2 hg38 chr7 522,595 525,244 2,650
ENST00000662957.3 hg38 chr7 522,553 525,240 2,688
ENST00000452622.1 hg38 chr7 520,391 525,232 4,842
ENST00000452622.1 hg19 chr7 560,028 564,869 4,842
ENST00000662957.3 hg19 chr7 562,190 564,877 2,688
ENST00000689546.2 hg19 chr7 562,232 564,881 2,650
ENST00000702988.1 hg19 chr7 562,233 564,870 2,638
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