SSX3 SSX family member 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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30 |
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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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Target data | : |
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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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MGeND data only
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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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Target data | : |
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 | CT5.3 |
MIM | 300325 OMIM |
HGNC | HGNC:11337 HGNC |
Ensembl | ENSG00000165584 Ensembl |
AllianceGenome | HGNC:11337 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000376893.7 | hg38 | chrX | 48,348,257 | 48,356,707 | 8,451 |
ENST00000298396.7 | hg38 | chrX | 48,346,427 | 48,356,703 | 10,277 |
ENST00000612497.1 | hg38 | chrX | 48,349,446 | 48,355,272 | 5,827 |
ENST00000298396.7 | hg19 | chrX | 48,205,862 | 48,216,138 | 10,277 |
ENST00000376893.7 | hg19 | chrX | 48,207,692 | 48,216,142 | 8,451 |
ENST00000612497.1 | hg19 | chrX | 48,208,881 | 48,214,707 | 5,827 |
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