CCT8 chaperonin containing TCP1 subunit 8
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 60 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
62 |
![]() |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | C21orf112 |
SYNONYM | Cctq |
SYNONYM | D21S246 |
SYNONYM | PRED71 |
MIM | 617786 OMIM |
HGNC | HGNC:1623 HGNC |
Ensembl | ENSG00000156261 Ensembl |
AllianceGenome | HGNC:1623 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000540844.5 | hg38 | chr21 | 29,056,322 | 29,073,797 | 17,476 |
ENST00000626972.2 | hg38 | chr21 | 29,056,329 | 29,073,351 | 17,023 |
ENST00000286788.9 | hg38 | chr21 | 29,056,326 | 29,073,648 | 17,323 |
ENST00000540844.5 | hg19 | chr21 | 30,428,643 | 30,446,118 | 17,476 |
ENST00000286788.9 | hg19 | chr21 | 30,428,647 | 30,445,969 | 17,323 |
ENST00000626972.2 | hg19 | chr21 | 30,428,650 | 30,445,672 | 17,023 |
Genome browser