FIGNL2-DT FIGNL2 divergent transcript

Information
Symbol
FIGNL2-DT
Type
ncRNA
Description
FIGNL2 divergent transcript
Entrez Gene ID
105369971
Genome
hg19
Position
chr12:52,242,007-52,246,513
Genome
hg38
Position
chr12:51,848,223-51,852,729
HGNC
HGNC:53299 HGNC
Ensembl
ENSG00000259887 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
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
[No Data.]
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:53299 HGNC
Ensembl ENSG00000259887 Ensembl
AllianceGenome HGNC:53299
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000562996.1 hg38 chr12 51,848,223 51,852,729 4,507
ENST00000562996.1 hg19 chr12 52,242,007 52,246,513 4,507
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