ENST00000662867.1 FIRRE

Information
Transcript ID
ENST00000662867.1
Genome
hg38
Position
chrX:131,689,738-131,785,262
Strand
-
CDS length
0
Amino acid length
0
Gene symbol
FIRRE
Gene type
ncRNA
Gene description
firre intergenic repeating RNA element
Gene Entrez Gene ID
286467
Variants

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Target data :
MGeND data only
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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
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MGeND data only
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Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
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MGeND data only
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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
Exon
Exon number Start Stop
10 131,689,738 131,689,840
9 131,689,946 131,690,015
8 131,692,438 131,692,636
7 131,749,306 131,749,458
6 131,755,598 131,755,746
5 131,756,611 131,756,709
4 131,768,549 131,768,696
3 131,777,623 131,777,744
2 131,783,887 131,784,039
1 131,785,157 131,785,262
Other genome
Genome Chromosome Start End Links
hg19 chrX 130,823,766 130,919,290 Link
CDS sequence
Amino sequence