CSNK2B casein kinase 2 beta
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 5 | 84 |
| Likely pathogenic | 0 | 66 |
| Benign | 0 | 16 |
| Likely benign | 0 | 16 |
| Conflicting classifications of pathogenicity | 0 | 8 |
| not provided | 2 | 2 |
| Uncertain significance | 0 | 62 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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18 |
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194 |
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18 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | CK2B |
| SYNONYM | CK2N |
| SYNONYM | CSK2B |
| SYNONYM | Ckb1 |
| SYNONYM | Ckb2 |
| SYNONYM | G5A |
| SYNONYM | POBINDS |
| MIM | 115441 OMIM |
| HGNC | HGNC:2460 HGNC |
| Ensembl | ENSG00000204435 Ensembl |
| AllianceGenome | HGNC:2460 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000677536.1 | hg38 | chr6 | 31,665,234 | 31,670,074 | 4,841 |
| ENST00000375885.8 | hg38 | chr6 | 31,665,236 | 31,670,070 | 4,835 |
| ENST00000375882.7 | hg38 | chr6 | 31,666,080 | 31,670,067 | 3,988 |
| ENST00000375866.2 | hg38 | chr6 | 31,666,355 | 31,670,070 | 3,716 |
| ENST00000375865.6 | hg38 | chr6 | 31,666,292 | 31,670,070 | 3,779 |
| ENST00000677536.1 | hg19 | chr6 | 31,633,011 | 31,637,851 | 4,841 |
| ENST00000375885.8 | hg19 | chr6 | 31,633,013 | 31,637,847 | 4,835 |
| ENST00000375882.7 | hg19 | chr6 | 31,633,857 | 31,637,844 | 3,988 |
| ENST00000375865.6 | hg19 | chr6 | 31,634,069 | 31,637,847 | 3,779 |
| ENST00000375866.2 | hg19 | chr6 | 31,634,132 | 31,637,847 | 3,716 |
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