RFX3-DT RFX3 divergent transcript

Information
Symbol
RFX3-DT
Type
ncRNA
Description
RFX3 divergent transcript
Entrez Gene ID
101929302
Genome
hg19
Position
chr9:3,526,535-3,674,931
Genome
hg38
Position
chr9:3,526,535-3,674,931
HGNC
HGNC:51197 HGNC
Ensembl
ENSG00000232104 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 CVAT7
SYNONYM RFX3-AS1
HGNC HGNC:51197 HGNC
Ensembl ENSG00000232104 Ensembl
AllianceGenome HGNC:51197
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000691026.1 hg38 chr9 3,526,500 3,556,308 29,809
ENST00000701201.1 hg38 chr9 3,526,535 3,674,931 148,397
ENST00000427722.2 hg38 chr9 3,668,165 3,691,814 23,650
ENST00000423112.2 hg38 chr9 3,526,723 3,671,634 144,912
ENST00000701837.1 hg38 chr9 3,526,485 3,603,029 76,545
ENST00000701837.1 hg19 chr9 3,526,485 3,603,029 76,545
ENST00000691026.1 hg19 chr9 3,526,500 3,556,308 29,809
ENST00000701201.1 hg19 chr9 3,526,535 3,674,931 148,397
ENST00000423112.2 hg19 chr9 3,526,723 3,671,634 144,912
ENST00000427722.2 hg19 chr9 3,668,165 3,691,814 23,650
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