CCT6B chaperonin containing TCP1 subunit 6B
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 58 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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62 |
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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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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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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 | CCT-zeta-2 |
SYNONYM | CCTZ-2 |
SYNONYM | Cctz2 |
SYNONYM | TCP-1-zeta-2 |
SYNONYM | TSA303 |
MIM | 610730 OMIM |
HGNC | HGNC:1621 HGNC |
Ensembl | ENSG00000132141 Ensembl |
AllianceGenome | HGNC:1621 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000421975.7 | hg38 | chr17 | 34,927,859 | 34,961,402 | 33,544 |
ENST00000314144.10 | hg38 | chr17 | 34,927,861 | 34,961,460 | 33,600 |
ENST00000436961.7 | hg38 | chr17 | 34,927,932 | 34,961,458 | 33,527 |
ENST00000421975.7 | hg19 | chr17 | 33,254,878 | 33,288,421 | 33,544 |
ENST00000314144.10 | hg19 | chr17 | 33,254,880 | 33,288,479 | 33,600 |
ENST00000436961.7 | hg19 | chr17 | 33,254,951 | 33,288,477 | 33,527 |
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