UQCC3 ubiquinol-cytochrome c reductase complex assembly factor 3
Information
- Symbol
- UQCC3
- Type
- protein-coding
- Description
- ubiquinol-cytochrome c reductase complex assembly factor 3
- Entrez Gene ID
- 790955
- Genome
- hg19
- Position
- chr11:62,437,745-62,441,049
- Genome
- hg38
- Position
- chr11:62,670,273-62,673,577
- MIM
- 616097 OMIM
- HGNC
- HGNC:34399 HGNC
- Ensembl
- ENSG00000204922 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Benign | 0 | 12 |
Likely benign | 0 | 20 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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10 |
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48 |
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2 |
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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
MGeND data only
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | C11orf83 |
SYNONYM | CCDS41658.1 |
SYNONYM | MC3DN9 |
SYNONYM | UNQ655 |
MIM | 616097 OMIM |
HGNC | HGNC:34399 HGNC |
Ensembl | ENSG00000204922 Ensembl |
AllianceGenome | HGNC:34399 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000531323.1 | hg38 | chr11 | 62,670,273 | 62,673,577 | 3,305 |
ENST00000377953.4 | hg38 | chr11 | 62,671,673 | 62,673,686 | 2,014 |
ENST00000531323.1 | hg19 | chr11 | 62,437,745 | 62,441,049 | 3,305 |
ENST00000377953.4 | hg19 | chr11 | 62,439,145 | 62,441,158 | 2,014 |
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