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 |
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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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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
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Category | : |
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Search word | : | |
Filtering | : |
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 |
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 |
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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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