SSX7 SSX family member 7

Information
Symbol
SSX7
Type
protein-coding
Description
SSX family member 7
Entrez Gene ID
280658
Genome
hg19
Position
chrX:52,673,111-52,683,950
Genome
hg38
Position
chrX:52,644,061-52,654,900
MIM
300542 OMIM
HGNC
HGNC:19653 HGNC
Ensembl
ENSG00000187754 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 10
not provided 6 0
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
50
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
MIM 300542 OMIM
HGNC HGNC:19653 HGNC
Ensembl ENSG00000187754 Ensembl
AllianceGenome HGNC:19653
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000298181.6 hg38 chrX 52,644,061 52,654,900 10,840
ENST00000298181.6 hg19 chrX 52,673,111 52,683,950 10,840
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