ARHGEF9-IT1 ARHGEF9 intronic transcript 1

Information
Symbol
ARHGEF9-IT1
Type
ncRNA
Description
ARHGEF9 intronic transcript 1
Entrez Gene ID
100874355
Genome
hg19
Position
chrX:62,890,076-62,891,382
Genome
hg38
Position
chrX:63,670,196-63,671,502
HGNC
HGNC:41401 HGNC
Ensembl
ENSG00000231729 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 0
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
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:41401 HGNC
Ensembl ENSG00000231729 Ensembl
AllianceGenome HGNC:41401
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000420917.1 hg38 chrX 63,670,196 63,671,502 1,307
ENST00000420917.1 hg19 chrX 62,890,076 62,891,382 1,307
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