FIRRE firre intergenic repeating RNA element

Information
Symbol
FIRRE
Type
ncRNA
Description
firre intergenic repeating RNA element
Entrez Gene ID
286467
Genome
hg19
Position
chrX:130,822,807-130,964,632
Genome
hg38
Position
chrX:131,688,779-131,830,604
MIM
300999 OMIM
HGNC
HGNC:49627 HGNC
Ensembl
ENSG00000213468 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
SYNONYM LINC01200
MIM 300999 OMIM
HGNC HGNC:49627 HGNC
Ensembl ENSG00000213468 Ensembl
AllianceGenome HGNC:49627
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000648028.2 hg38 chrX 131,694,861 131,794,142 99,282
ENST00000649541.1 hg38 chrX 131,688,779 131,830,604 141,826
ENST00000637577.2 hg38 chrX 131,691,530 131,795,809 104,280
ENST00000427391.2 hg38 chrX 131,702,652 131,830,643 127,992
ENST00000662867.1 hg38 chrX 131,689,738 131,785,262 95,525
ENST00000649391.1 hg38 chrX 131,691,996 131,785,262 93,267
ENST00000649541.1 hg19 chrX 130,822,807 130,964,632 141,826
ENST00000637577.2 hg19 chrX 130,825,558 130,929,837 104,280
ENST00000649391.1 hg19 chrX 130,826,024 130,919,290 93,267
ENST00000648028.2 hg19 chrX 130,828,889 130,928,170 99,282
ENST00000427391.2 hg19 chrX 130,836,680 130,964,671 127,992
ENST00000662867.1 hg19 chrX 130,823,766 130,919,290 95,525
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