CD37 CD37 molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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
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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 | GP52-40 |
SYNONYM | TSPAN26 |
MIM | 151523 OMIM |
HGNC | HGNC:1666 HGNC |
Ensembl | ENSG00000104894 Ensembl |
AllianceGenome | HGNC:1666 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000535669.6 | hg38 | chr19 | 49,335,427 | 49,340,205 | 4,779 |
ENST00000323906.9 | hg38 | chr19 | 49,335,406 | 49,340,606 | 5,201 |
ENST00000598095.5 | hg38 | chr19 | 49,335,396 | 49,340,132 | 4,737 |
ENST00000426897.6 | hg38 | chr19 | 49,335,396 | 49,340,575 | 5,180 |
ENST00000598095.5 | hg19 | chr19 | 49,838,653 | 49,843,389 | 4,737 |
ENST00000426897.6 | hg19 | chr19 | 49,838,653 | 49,843,832 | 5,180 |
ENST00000323906.9 | hg19 | chr19 | 49,838,663 | 49,843,863 | 5,201 |
ENST00000535669.6 | hg19 | chr19 | 49,838,684 | 49,843,462 | 4,779 |
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