TSPAN18 tetraspanin 18
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 34 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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50 |
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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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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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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 | TSPAN |
MIM | 619399 OMIM |
HGNC | HGNC:20660 HGNC |
Ensembl | ENSG00000157570 Ensembl |
AllianceGenome | HGNC:20660 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000340160.7 | hg38 | chr11 | 44,764,426 | 44,932,421 | 167,996 |
ENST00000520358.7 | hg38 | chr11 | 44,726,962 | 44,932,423 | 205,462 |
ENST00000520358.7 | hg19 | chr11 | 44,748,512 | 44,953,974 | 205,463 |
ENST00000340160.7 | hg19 | chr11 | 44,785,976 | 44,953,972 | 167,997 |
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