ENST00000649541.1 FIRRE

Information
Transcript ID
ENST00000649541.1
Genome
hg38
Position
chrX:131,688,779-131,830,604
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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Target data :
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
12 131,688,779 131,692,636
11 131,749,306 131,749,458
10 131,755,598 131,755,746
9 131,756,611 131,756,709
8 131,768,549 131,768,696
7 131,777,623 131,777,744
6 131,783,887 131,784,039
5 131,785,157 131,785,258
4 131,793,994 131,794,115
3 131,794,324 131,794,466
2 131,825,222 131,825,365
1 131,830,292 131,830,604
Other genome
Genome Chromosome Start End Links
hg19 chrX 130,822,807 130,964,632 Link
CDS sequence
Amino sequence