TSPAN16 tetraspanin 16
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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26 |
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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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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 | TM-8 |
SYNONYM | TM4-B |
SYNONYM | TM4SF16 |
MIM | 617580 OMIM |
HGNC | HGNC:30725 HGNC |
Ensembl | ENSG00000130167 Ensembl |
AllianceGenome | HGNC:30725 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000621731.4 | hg38 | chr19 | 11,296,139 | 11,306,603 | 10,465 |
ENST00000592955.5 | hg38 | chr19 | 11,296,160 | 11,315,967 | 19,808 |
ENST00000590327.6 | hg38 | chr19 | 11,296,160 | 11,315,967 | 19,808 |
ENST00000316737.5 | hg38 | chr19 | 11,296,148 | 11,326,996 | 30,849 |
ENST00000621731.4 | hg19 | chr19 | 11,406,815 | 11,417,279 | 10,465 |
ENST00000316737.5 | hg19 | chr19 | 11,406,824 | 11,437,672 | 30,849 |
ENST00000590327.6 | hg19 | chr19 | 11,406,836 | 11,426,643 | 19,808 |
ENST00000592955.5 | hg19 | chr19 | 11,406,836 | 11,426,643 | 19,808 |
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