TNFRSF8 TNF receptor superfamily member 8
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Likely benign | 0 | 14 |
not provided | 17 | 0 |
Uncertain significance | 0 | 68 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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90 |
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2 |
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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Search word | : | |
Filtering | : |
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 | CD30 |
SYNONYM | D1S166E |
SYNONYM | Ki-1 |
MIM | 153243 OMIM |
HGNC | HGNC:11923 HGNC |
Ensembl | ENSG00000120949 Ensembl |
AllianceGenome | HGNC:11923 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000413146.6 | hg38 | chr1 | 12,125,899 | 12,144,207 | 18,309 |
ENST00000263932.7 | hg38 | chr1 | 12,063,303 | 12,144,207 | 80,905 |
ENST00000417814.3 | hg38 | chr1 | 12,063,377 | 12,144,205 | 80,829 |
ENST00000263932.7 | hg19 | chr1 | 12,123,360 | 12,204,264 | 80,905 |
ENST00000417814.3 | hg19 | chr1 | 12,123,434 | 12,204,262 | 80,829 |
ENST00000413146.6 | hg19 | chr1 | 12,185,956 | 12,204,264 | 18,309 |
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