CD7 CD7 molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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34 |
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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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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 | GP40 |
SYNONYM | LEU-9 |
SYNONYM | TP41 |
SYNONYM | Tp40 |
MIM | 186820 OMIM |
HGNC | HGNC:1695 HGNC |
Ensembl | ENSG00000173762 Ensembl |
AllianceGenome | HGNC:1695 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000583376.1 | hg38 | chr17 | 82,314,874 | 82,317,552 | 2,679 |
ENST00000312648.8 | hg38 | chr17 | 82,314,873 | 82,317,608 | 2,736 |
ENST00000578509.1 | hg38 | chr17 | 82,315,975 | 82,317,558 | 1,584 |
ENST00000584284.5 | hg38 | chr17 | 82,314,868 | 82,317,577 | 2,710 |
ENST00000584284.5 | hg19 | chr17 | 80,272,744 | 80,275,453 | 2,710 |
ENST00000312648.8 | hg19 | chr17 | 80,272,749 | 80,275,484 | 2,736 |
ENST00000583376.1 | hg19 | chr17 | 80,272,750 | 80,275,428 | 2,679 |
ENST00000578509.1 | hg19 | chr17 | 80,273,851 | 80,275,434 | 1,584 |
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