HNRNPUL2-BSCL2 HNRNPUL2-BSCL2 readthrough (NMD candidate)

Information
Symbol
HNRNPUL2-BSCL2
Type
ncRNA
Description
HNRNPUL2-BSCL2 readthrough (NMD candidate)
Entrez Gene ID
100534595
Genome
hg19
Position
chr11:62,457,747-62,494,856
Genome
hg38
Position
chr11:62,690,275-62,727,384
HGNC
HGNC:49189 HGNC
Ensembl
ENSG00000234857 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 64
Likely pathogenic 0 34
Benign 10 50
Likely benign 0 342
Conflicting classifications of pathogenicity 0 92
not provided 0 2
Uncertain significance 0 578
Ranking
ClinVar
0
0
240
772
44
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
HGNC HGNC:49189 HGNC
Ensembl ENSG00000234857 Ensembl
AllianceGenome HGNC:49189
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000403734.2 hg38 chr11 62,690,275 62,727,384 37,110
ENST00000403734.2 hg19 chr11 62,457,747 62,494,856 37,110
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