TROAP trophinin associated protein
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 18 |
Uncertain significance | 0 | 96 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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114 |
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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 |
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SYNONYM | TASTIN |
MIM | 603872 OMIM |
HGNC | HGNC:12327 HGNC |
Ensembl | ENSG00000135451 Ensembl |
AllianceGenome | HGNC:12327 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000547923.1 | hg38 | chr12 | 49,326,641 | 49,331,708 | 5,068 |
ENST00000548311.5 | hg38 | chr12 | 49,323,255 | 49,324,416 | 1,162 |
ENST00000380327.9 | hg38 | chr12 | 49,323,255 | 49,324,392 | 1,138 |
ENST00000551245.5 | hg38 | chr12 | 49,323,244 | 49,331,670 | 8,427 |
ENST00000550709.5 | hg38 | chr12 | 49,323,257 | 49,324,380 | 1,124 |
ENST00000257909.8 | hg38 | chr12 | 49,323,255 | 49,331,731 | 8,477 |
ENST00000549534.1 | hg38 | chr12 | 49,323,273 | 49,324,365 | 1,093 |
ENST00000549275.5 | hg38 | chr12 | 49,323,236 | 49,324,296 | 1,061 |
ENST00000549275.5 | hg19 | chr12 | 49,717,019 | 49,718,079 | 1,061 |
ENST00000551245.5 | hg19 | chr12 | 49,717,027 | 49,725,453 | 8,427 |
ENST00000380327.9 | hg19 | chr12 | 49,717,038 | 49,718,175 | 1,138 |
ENST00000548311.5 | hg19 | chr12 | 49,717,038 | 49,718,199 | 1,162 |
ENST00000257909.8 | hg19 | chr12 | 49,717,038 | 49,725,514 | 8,477 |
ENST00000550709.5 | hg19 | chr12 | 49,717,040 | 49,718,163 | 1,124 |
ENST00000549534.1 | hg19 | chr12 | 49,717,056 | 49,718,148 | 1,093 |
ENST00000547923.1 | hg19 | chr12 | 49,720,424 | 49,725,491 | 5,068 |
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