TRAF6 TNF receptor associated factor 6
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 10 |
not provided | 1 | 0 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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40 |
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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 |
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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 |
Search Word
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 | MGC:3310 |
SYNONYM | RNF85 |
MIM | 602355 OMIM |
HGNC | HGNC:12036 HGNC |
Ensembl | ENSG00000175104 Ensembl |
AllianceGenome | HGNC:12036 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000348124.5 | hg38 | chr11 | 36,489,173 | 36,510,256 | 21,084 |
ENST00000526995.6 | hg38 | chr11 | 36,483,769 | 36,510,272 | 26,504 |
ENST00000526995.6 | hg19 | chr11 | 36,505,319 | 36,531,822 | 26,504 |
ENST00000348124.5 | hg19 | chr11 | 36,510,723 | 36,531,806 | 21,084 |
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