PTCRA pre T cell antigen receptor alpha
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 36 |
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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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 |
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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 |
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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 | PT-ALPHA |
SYNONYM | PTA |
MIM | 606817 OMIM |
HGNC | HGNC:21290 HGNC |
Ensembl | ENSG00000171611 Ensembl |
AllianceGenome | HGNC:21290 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000616441.2 | hg38 | chr6 | 42,915,989 | 42,925,835 | 9,847 |
ENST00000441198.4 | hg38 | chr6 | 42,915,989 | 42,925,835 | 9,847 |
ENST00000446507.5 | hg38 | chr6 | 42,915,989 | 42,925,835 | 9,847 |
ENST00000304672.6 | hg38 | chr6 | 42,916,053 | 42,925,838 | 9,786 |
ENST00000441198.4 | hg19 | chr6 | 42,883,727 | 42,893,573 | 9,847 |
ENST00000446507.5 | hg19 | chr6 | 42,883,727 | 42,893,573 | 9,847 |
ENST00000616441.2 | hg19 | chr6 | 42,883,727 | 42,893,573 | 9,847 |
ENST00000304672.6 | hg19 | chr6 | 42,883,791 | 42,893,576 | 9,786 |
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