CCT3 chaperonin containing TCP1 subunit 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 1 |
Benign | 0 | 2 |
Uncertain significance | 0 | 62 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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64 |
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1 |
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 | CCT-gamma |
SYNONYM | CCTG |
SYNONYM | PIG48 |
SYNONYM | TCP-1-gamma |
SYNONYM | TRIC5 |
MIM | 600114 OMIM |
HGNC | HGNC:1616 HGNC |
Ensembl | ENSG00000163468 Ensembl |
AllianceGenome | HGNC:1616 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000368259.6 | hg38 | chr1 | 156,308,969 | 156,338,245 | 29,277 |
ENST00000472765.6 | hg38 | chr1 | 156,309,165 | 156,338,257 | 29,093 |
ENST00000295688.8 | hg38 | chr1 | 156,308,968 | 156,338,292 | 29,325 |
ENST00000295688.8 | hg19 | chr1 | 156,278,759 | 156,308,083 | 29,325 |
ENST00000368259.6 | hg19 | chr1 | 156,278,760 | 156,308,036 | 29,277 |
ENST00000472765.6 | hg19 | chr1 | 156,278,956 | 156,308,048 | 29,093 |
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