ZNF692-DT ZNF692 divergent transcript

Information
Symbol
ZNF692-DT
Type
ncRNA
Description
ZNF692 divergent transcript
Entrez Gene ID
122152365
Genome
hg19
Position
chr1:249,153,363-249,158,995
Genome
hg38
Position
chr1:248,859,164-248,864,796
HGNC
HGNC:55817 HGNC
Ensembl
ENSG00000227237 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:55817 HGNC
Ensembl ENSG00000227237 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000417047.1 hg38 chr1 248,859,164 248,864,796 5,633
ENST00000417047.1 hg19 chr1 249,153,363 249,158,995 5,633
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