TNF tumor necrosis factor
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Benign | 0 | 4 |
Likely benign | 0 | 10 |
not provided | 1 | 0 |
Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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18 |
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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
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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 |
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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 | DIF |
SYNONYM | TNF-alpha |
SYNONYM | TNFA |
SYNONYM | TNFSF2 |
SYNONYM | TNLG1F |
MIM | 191160 OMIM |
HGNC | HGNC:11892 HGNC |
Ensembl | ENSG00000232810 Ensembl |
AllianceGenome | HGNC:11892 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000449264.3 | hg38 | chr6 | 31,575,565 | 31,578,336 | 2,772 |
ENST00000699334.1 | hg38 | chr6 | 31,575,742 | 31,577,537 | 1,796 |
ENST00000449264.3 | hg19 | chr6 | 31,543,342 | 31,546,113 | 2,772 |
ENST00000699334.1 | hg19 | chr6 | 31,543,519 | 31,545,314 | 1,796 |
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