C6orf47 chromosome 6 open reading frame 47
Information
- Symbol
- C6orf47
- Type
- protein-coding
- Description
- chromosome 6 open reading frame 47
- Entrez Gene ID
- 57827
- Genome
- hg19
- Position
- chr6:31,626,075-31,628,555
- Genome
- hg38
- Position
- chr6:31,658,298-31,660,778
- HGNC
- HGNC:19076 HGNC
- Ensembl
- ENSG00000204439 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 1 | 0 |
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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4 |
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0 |
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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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 |
Search Word
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 | D6S53E |
SYNONYM | G4 |
SYNONYM | NG34 |
HGNC | HGNC:19076 HGNC |
Ensembl | ENSG00000204439 Ensembl |
AllianceGenome | HGNC:19076 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000375911.2 | hg38 | chr6 | 31,658,298 | 31,660,778 | 2,481 |
ENST00000375911.2 | hg19 | chr6 | 31,626,075 | 31,628,555 | 2,481 |
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