SLX1B-SULT1A4 SLX1B-SULT1A4 readthrough (NMD candidate)

Information
Symbol
SLX1B-SULT1A4
Type
ncRNA
Description
SLX1B-SULT1A4 readthrough (NMD candidate)
Entrez Gene ID
100526831
Genome
hg19
Position
chr16:29,466,426-29,476,094
Genome
hg38
Position
chr16:29,455,105-29,464,773
HGNC
HGNC:48353 HGNC
Ensembl
ENSG00000260280 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 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
HGNC HGNC:48353 HGNC
Ensembl ENSG00000260280 Ensembl
AllianceGenome HGNC:48353
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000344620.10 hg38 chr16 29,455,105 29,464,773 9,669
ENST00000344620.10 hg19 chr16 29,466,426 29,476,094 9,669
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