TM4SF19-DYNLT2B TM4SF19-DYNLT2B readthrough (NMD candidate)

Information
Symbol
TM4SF19-DYNLT2B
Type
ncRNA
Description
TM4SF19-DYNLT2B readthrough (NMD candidate)
Entrez Gene ID
100534611
HGNC
HGNC:49190 HGNC
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
0
Frequency
[No Data.]
Disease area statistics
[No Data.]
Locus Zoom
[No Data.]
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 TM4SF19-TCTEX1D2
HGNC HGNC:49190 HGNC
AllianceGenome HGNC:49190
DescrptionSourceLinks
Genome browser
[No Data.]