TBC1D3C TBC1 domain family member 3C
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 1 |
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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25 |
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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
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 |
Search Word
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 | PRC17 |
SYNONYM | TBC1D3 |
SYNONYM | TBC1D3A |
SYNONYM | TBC1D3D |
MIM | 610806 OMIM |
HGNC | HGNC:24889 HGNC |
Ensembl | ENSG00000278299 Ensembl |
AllianceGenome | HGNC:24889 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000622206.2 | hg38 | chr17 | 38,057,693 | 38,068,634 | 10,942 |
ENST00000622206.2 | hg19 | chr17 | 34,746,236 | 34,757,033 | 10,798 |
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