TSPAN9 tetraspanin 9
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 2 | 0 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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32 |
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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
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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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 | NET-5 |
SYNONYM | NET5 |
SYNONYM | PP1057 |
MIM | 613137 OMIM |
HGNC | HGNC:21640 HGNC |
Ensembl | ENSG00000011105 Ensembl |
AllianceGenome | HGNC:21640 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000537971.5 | hg38 | chr12 | 3,077,355 | 3,286,564 | 209,210 |
ENST00000011898.10 | hg38 | chr12 | 3,077,379 | 3,286,559 | 209,181 |
ENST00000407263.2 | hg38 | chr12 | 3,201,177 | 3,282,108 | 80,932 |
ENST00000537971.5 | hg19 | chr12 | 3,186,521 | 3,395,730 | 209,210 |
ENST00000011898.10 | hg19 | chr12 | 3,186,545 | 3,395,725 | 209,181 |
ENST00000407263.2 | hg19 | chr12 | 3,310,343 | 3,391,274 | 80,932 |
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