TSPO2 translocator protein 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
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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12 |
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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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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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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 | BZRPL1 |
MIM | 619409 OMIM |
HGNC | HGNC:21256 HGNC |
Ensembl | ENSG00000112212 Ensembl |
AllianceGenome | HGNC:21256 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000373161.6 | hg38 | chr6 | 41,042,467 | 41,044,337 | 1,871 |
ENST00000373158.6 | hg38 | chr6 | 41,042,571 | 41,044,256 | 1,686 |
ENST00000470917.1 | hg38 | chr6 | 41,042,718 | 41,044,212 | 1,495 |
ENST00000373161.6 | hg19 | chr6 | 41,010,206 | 41,012,076 | 1,871 |
ENST00000373158.6 | hg19 | chr6 | 41,010,310 | 41,011,995 | 1,686 |
ENST00000470917.1 | hg19 | chr6 | 41,010,457 | 41,011,951 | 1,495 |
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