CD82 CD82 molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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38 |
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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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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 | 4F9 |
SYNONYM | C33 |
SYNONYM | GR15 |
SYNONYM | IA4 |
SYNONYM | KAI1 |
SYNONYM | R2 |
SYNONYM | SAR2 |
SYNONYM | ST6 |
SYNONYM | TSPAN27 |
MIM | 600623 OMIM |
HGNC | HGNC:6210 HGNC |
Ensembl | ENSG00000085117 Ensembl |
AllianceGenome | HGNC:6210 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000227155.9 | hg38 | chr11 | 44,565,663 | 44,620,358 | 54,696 |
ENST00000342935.7 | hg38 | chr11 | 44,565,601 | 44,619,126 | 53,526 |
ENST00000342935.7 | hg19 | chr11 | 44,587,151 | 44,640,676 | 53,526 |
ENST00000227155.9 | hg19 | chr11 | 44,587,213 | 44,641,908 | 54,696 |
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