BRCC3 BRCA1/BRCA2-containing complex subunit 3
Information
- Symbol
- BRCC3
- Type
- protein-coding
- Description
- BRCA1/BRCA2-containing complex subunit 3
- Entrez Gene ID
- 79184
- Genome
- hg19
- Position
- chrX:154,299,778-154,351,349
- Genome
- hg38
- Position
- chrX:155,071,503-155,123,074
- MIM
- 300617 OMIM
- HGNC
- HGNC:24185 HGNC
- Ensembl
- ENSG00000185515 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 16 |
| not provided | 10 | 0 |
| Uncertain significance | 0 | 6 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
![]() |
8 |
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16 |
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
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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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 | BRCC36 |
| SYNONYM | C6.1A |
| SYNONYM | CXorf53 |
| MIM | 300617 OMIM |
| HGNC | HGNC:24185 HGNC |
| Ensembl | ENSG00000185515 Ensembl |
| AllianceGenome | HGNC:24185 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000330045.12 | hg38 | chrX | 155,071,508 | 155,123,077 | 51,570 |
| ENST00000369462.5 | hg38 | chrX | 155,071,503 | 155,123,074 | 51,572 |
| ENST00000340647.8 | hg38 | chrX | 155,071,420 | 155,121,318 | 49,899 |
| ENST00000369459.6 | hg38 | chrX | 155,071,499 | 155,123,072 | 51,574 |
| ENST00000340647.8 | hg19 | chrX | 154,299,695 | 154,349,593 | 49,899 |
| ENST00000369459.6 | hg19 | chrX | 154,299,774 | 154,351,347 | 51,574 |
| ENST00000369462.5 | hg19 | chrX | 154,299,778 | 154,351,349 | 51,572 |
| ENST00000330045.12 | hg19 | chrX | 154,299,783 | 154,351,352 | 51,570 |
| Key | Value |
|---|---|
| strand | + |
| UniProt | OG |
| start | 154,299,694 |
| Gene Symbol | BRCC3 |
| Entrez GeneId | 79,184 |
| Chr Band | Xq28 |
| end | 154,351,348 |
| chr | chrX |
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