PIWIL2-DT PIWIL2 divergent transcript

Information
Symbol
PIWIL2-DT
Type
ncRNA
Description
PIWIL2 divergent transcript
Entrez Gene ID
100507071
Genome
hg19
Position
chr8:22,112,089-22,132,675
Genome
hg38
Position
chr8:22,254,576-22,275,162
HGNC
HGNC:55522 HGNC
Ensembl
ENSG00000254064 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:55522 HGNC
Ensembl ENSG00000254064 Ensembl
AllianceGenome HGNC:55522
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000523556.1 hg38 chr8 22,254,576 22,275,162 20,587
ENST00000523556.1 hg19 chr8 22,112,089 22,132,675 20,587
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