TNFSF8 TNF superfamily member 8
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 1 | 0 |
Likely benign | 0 | 4 |
not provided | 65 | 0 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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18 |
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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
Search Word
Target data | : |
MGeND data only
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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 |
Search Word
Target data | : |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | CD153 |
SYNONYM | CD30L |
SYNONYM | CD30LG |
SYNONYM | TNLG3A |
MIM | 603875 OMIM |
HGNC | HGNC:11938 HGNC |
Ensembl | ENSG00000106952 Ensembl |
AllianceGenome | HGNC:11938 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000223795.3 | hg38 | chr9 | 114,901,145 | 114,930,591 | 29,447 |
ENST00000618336.4 | hg38 | chr9 | 114,893,343 | 114,930,595 | 37,253 |
ENST00000618336.4 | hg19 | chr9 | 117,655,623 | 117,692,875 | 37,253 |
ENST00000223795.3 | hg19 | chr9 | 117,663,425 | 117,692,871 | 29,447 |
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