TRIP10 thyroid hormone receptor interactor 10
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 88 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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96 |
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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 | CIP4 |
SYNONYM | HSTP |
SYNONYM | STOT |
SYNONYM | STP |
SYNONYM | TRIP-10 |
MIM | 604504 OMIM |
HGNC | HGNC:12304 HGNC |
Ensembl | ENSG00000125733 Ensembl |
AllianceGenome | HGNC:12304 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000596758.5 | hg38 | chr19 | 6,739,762 | 6,751,464 | 11,703 |
ENST00000313244.14 | hg38 | chr19 | 6,739,680 | 6,751,530 | 11,851 |
ENST00000600428.5 | hg38 | chr19 | 6,737,925 | 6,751,500 | 13,576 |
ENST00000313285.12 | hg38 | chr19 | 6,739,680 | 6,751,526 | 11,847 |
ENST00000600428.5 | hg19 | chr19 | 6,737,936 | 6,751,511 | 13,576 |
ENST00000313285.12 | hg19 | chr19 | 6,739,691 | 6,751,537 | 11,847 |
ENST00000313244.14 | hg19 | chr19 | 6,739,691 | 6,751,541 | 11,851 |
ENST00000596758.5 | hg19 | chr19 | 6,739,773 | 6,751,475 | 11,703 |
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