SSX4 SSX family member 4
Clinical Significance
MGeND | ClinVar | |
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Likely benign | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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8 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | CT5.4 |
MIM | 300326 OMIM |
HGNC | HGNC:11338 HGNC |
Ensembl | ENSG00000268009 Ensembl |
AllianceGenome | HGNC:11338 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000620320.4 | hg38 | chrX | 48,383,516 | 48,393,343 | 9,828 |
ENST00000595689.3 | hg38 | chrX | 48,383,539 | 48,393,347 | 9,809 |
ENST00000620320.4 | hg19 | chrX | 48,242,957 | 48,252,785 | 9,829 |
ENST00000595689.3 | hg19 | chrX | 48,242,980 | 48,252,789 | 9,810 |
Key | Value |
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strand | + |
start | 48,242,967 |
Gene Symbol | SSX4 |
Entrez GeneId | 6,759 |
Chr Band | Xp11.23 |
end | 48,271,343 |
chr | chrX |
Name | synovial sarcoma, X breakpoint 4 |
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