BICRA BRD4 interacting chromatin remodeling complex associated protein
Information
- Symbol
- BICRA
- Type
- protein-coding
- Description
- BRD4 interacting chromatin remodeling complex associated protein
- Entrez Gene ID
- 29998
- Genome
- hg19
- Position
- chr19:48,111,453-48,206,534
- Genome
- hg38
- Position
- chr19:47,608,196-47,703,277
- MIM
- 605690 OMIM
- HGNC
- HGNC:4332 HGNC
- Ensembl
- ENSG00000063169 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 26 |
| Likely pathogenic | 0 | 16 |
| Benign | 0 | 38 |
| Likely benign | 0 | 74 |
| Conflicting classifications of pathogenicity | 0 | 22 |
| Uncertain significance | 0 | 392 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
36 |
 |
502 |
 |
8 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| 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
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| Category | : |
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| 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 | CSS12 |
| SYNONYM | GLTSCR1 |
| SYNONYM | SMARCK1 |
| MIM | 605690 OMIM |
| HGNC | HGNC:4332 HGNC |
| Ensembl | ENSG00000063169 Ensembl |
| AllianceGenome | HGNC:4332 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000396720.7 | hg38 | chr19 | 47,608,196 | 47,703,277 | 95,082 |
| ENST00000594866.3 | hg38 | chr19 | 47,609,134 | 47,703,277 | 94,144 |
| ENST00000614245.2 | hg38 | chr19 | 47,678,962 | 47,703,222 | 24,261 |
| ENST00000396720.7 | hg19 | chr19 | 48,111,453 | 48,206,534 | 95,082 |
| ENST00000594866.3 | hg19 | chr19 | 48,112,391 | 48,206,534 | 94,144 |
| ENST00000614245.2 | hg19 | chr19 | 48,182,219 | 48,206,479 | 24,261 |
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