SSX2B SSX family member 2B

Information
Symbol
SSX2B
Type
protein-coding
Description
SSX family member 2B
Entrez Gene ID
727837
Genome
hg19
Position
chrX:52,780,346-52,790,617
Genome
hg38
Position
chrX:52,751,269-52,761,536
HGNC
HGNC:22263 HGNC
Ensembl
ENSG00000268447 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
SYNONYM CT5.2
SYNONYM CT5.2b
SYNONYM HOM-MEL-40
SYNONYM SSX
HGNC HGNC:22263 HGNC
Ensembl ENSG00000268447 Ensembl
AllianceGenome HGNC:22263
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000616191.4 hg38 chrX 52,751,132 52,790,305 39,174
ENST00000596480.6 hg38 chrX 52,751,252 52,761,536 10,285
ENST00000612490.1 hg38 chrX 52,751,269 52,761,536 10,268
ENST00000616191.4 hg19 chrX 52,780,209 52,819,350 39,142
ENST00000596480.6 hg19 chrX 52,780,329 52,790,617 10,289
ENST00000612490.1 hg19 chrX 52,780,346 52,790,617 10,272
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