TRAF1 TNF receptor associated factor 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 1 | 0 |
Benign | 0 | 4 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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42 |
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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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Search word | : | |
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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 | EBI6 |
SYNONYM | MGC:10353 |
MIM | 601711 OMIM |
HGNC | HGNC:12031 HGNC |
Ensembl | ENSG00000056558 Ensembl |
AllianceGenome | HGNC:12031 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000373887.8 | hg38 | chr9 | 120,902,393 | 120,926,796 | 24,404 |
ENST00000546084.5 | hg38 | chr9 | 120,902,393 | 120,914,572 | 12,180 |
ENST00000540010.1 | hg38 | chr9 | 120,902,393 | 120,929,173 | 26,781 |
ENST00000546084.5 | hg19 | chr9 | 123,664,671 | 123,676,850 | 12,180 |
ENST00000373887.8 | hg19 | chr9 | 123,664,671 | 123,689,074 | 24,404 |
ENST00000540010.1 | hg19 | chr9 | 123,664,671 | 123,691,451 | 26,781 |
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