FGF13-AS1 FGF13 antisense RNA 1

Information
Symbol
FGF13-AS1
Type
ncRNA
Description
FGF13 antisense RNA 1
Entrez Gene ID
100129662
Genome
hg19
Position
chrX:137,794,269-137,798,779
Genome
hg38
Position
chrX:138,712,107-138,716,617
MIM
301087 OMIM
HGNC
HGNC:44264 HGNC
Ensembl
ENSG00000226031 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
MIM 301087 OMIM
HGNC HGNC:44264 HGNC
Ensembl ENSG00000226031 Ensembl
AllianceGenome HGNC:44264
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000438238.1 hg38 chrX 138,712,107 138,716,617 4,511
ENST00000446383.5 hg38 chrX 138,711,452 138,716,092 4,641
ENST00000446383.5 hg19 chrX 137,793,614 137,798,254 4,641
ENST00000438238.1 hg19 chrX 137,794,269 137,798,779 4,511
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