CD27 CD27 molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 18 |
Likely pathogenic | 0 | 8 |
Benign | 0 | 18 |
Likely benign | 0 | 152 |
Conflicting classifications of pathogenicity | 0 | 8 |
Uncertain significance | 0 | 192 |
Ranking
ClinVar | |
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0 |
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0 |
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48 |
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332 |
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4 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
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 | S152 |
SYNONYM | S152. LPFS2 |
SYNONYM | T14 |
SYNONYM | TNFRSF7 |
SYNONYM | Tp55 |
MIM | 186711 OMIM |
HGNC | HGNC:11922 HGNC |
Ensembl | ENSG00000139193 Ensembl |
AllianceGenome | HGNC:11922 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000266557.4 | hg38 | chr12 | 6,444,955 | 6,451,713 | 6,759 |
ENST00000266557.4 | hg19 | chr12 | 6,554,121 | 6,560,879 | 6,759 |
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