TRAM1L1 translocation associated membrane protein 1 like 1
Information
- Symbol
- TRAM1L1
- Type
- protein-coding
- Description
- translocation associated membrane protein 1 like 1
- Entrez Gene ID
- 133022
- Genome
- hg19
- Position
- chr4:118,004,710-118,006,732
- Genome
- hg38
- Position
- chr4:117,083,554-117,085,576
- MIM
- 617505 OMIM
- HGNC
- HGNC:28371 HGNC
- Ensembl
- ENSG00000174599 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
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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36 |
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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 |
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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 |
---|---|
MIM | 617505 OMIM |
HGNC | HGNC:28371 HGNC |
Ensembl | ENSG00000174599 Ensembl |
AllianceGenome | HGNC:28371 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000310754.5 | hg38 | chr4 | 117,083,554 | 117,085,576 | 2,023 |
ENST00000310754.5 | hg19 | chr4 | 118,004,710 | 118,006,732 | 2,023 |
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