TRIM77 tripartite motif containing 77
Information
- Symbol
- TRIM77
- Type
- protein-coding
- Description
- tripartite motif containing 77
- Entrez Gene ID
- 390231
- Genome
- hg19
- Position
- chr11:89,443,467-89,451,040
- Genome
- hg38
- Position
- chr11:89,710,299-89,717,872
- HGNC
- HGNC:34228 HGNC
- Ensembl
- ENSG00000214414 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 62 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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64 |
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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 |
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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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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 | TRIM77P |
HGNC | HGNC:34228 HGNC |
Ensembl | ENSG00000214414 Ensembl |
AllianceGenome | HGNC:34228 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000398290.7 | hg38 | chr11 | 89,710,299 | 89,717,872 | 7,574 |
ENST00000398290.7 | hg19 | chr11 | 89,443,467 | 89,451,040 | 7,574 |
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