TRIM73 tripartite motif containing 73
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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10 |
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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 |
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 | : | |
Filtering | : |
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 |
---|---|
SYNONYM | TRIM50B |
MIM | 612549 OMIM |
HGNC | HGNC:18162 HGNC |
Ensembl | ENSG00000178809 Ensembl |
AllianceGenome | HGNC:18162 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000447409.6 | hg38 | chr7 | 75,398,142 | 75,405,605 | 7,464 |
ENST00000430211.5 | hg38 | chr7 | 75,395,756 | 75,410,996 | 15,241 |
ENST00000323819.8 | hg38 | chr7 | 75,395,629 | 75,405,605 | 9,977 |
ENST00000450434.5 | hg38 | chr7 | 75,395,063 | 75,405,613 | 10,551 |
ENST00000450434.1 | hg19 | chr7 | 75,024,337 | 75,034,896 | 10,560 |
ENST00000463766.1 | hg19 | chr7 | 75,024,435 | 75,028,314 | 3,880 |
ENST00000323819.3 | hg19 | chr7 | 75,024,903 | 75,034,888 | 9,986 |
ENST00000430211.1 | hg19 | chr7 | 75,025,030 | 75,040,279 | 15,250 |
ENST00000447409.2 | hg19 | chr7 | 75,027,418 | 75,034,888 | 7,471 |
ENST00000437796.1 | hg19 | chr7 | 75,028,199 | 75,034,888 | 6,690 |
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