TRADD TNFRSF1A associated via death domain
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
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
[No Data.]
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 |
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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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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 | Hs.89862 |
MIM | 603500 OMIM |
HGNC | HGNC:12030 HGNC |
Ensembl | ENSG00000102871 Ensembl |
AllianceGenome | HGNC:12030 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000486556.1 | hg38 | chr16 | 67,154,199 | 67,156,249 | 2,051 |
ENST00000345057.9 | hg38 | chr16 | 67,154,185 | 67,159,909 | 5,725 |
ENST00000345057.9 | hg19 | chr16 | 67,188,088 | 67,193,812 | 5,725 |
ENST00000486556.1 | hg19 | chr16 | 67,188,102 | 67,190,152 | 2,051 |
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