C13orf42 chromosome 13 open reading frame 42
Information
- Symbol
- C13orf42
- Type
- protein-coding
- Description
- chromosome 13 open reading frame 42
- Entrez Gene ID
- 647166
- Genome
- hg19
- Position
- chr13:51,656,255-51,685,410
- Genome
- hg38
- Position
- chr13:51,082,119-51,111,274
- HGNC
- HGNC:42693 HGNC
- Ensembl
- ENSG00000226792 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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 |
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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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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 |
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SYNONYM | LINC00371 |
SYNONYM | LINC00372 |
HGNC | HGNC:42693 HGNC |
Ensembl | ENSG00000226792 Ensembl |
AllianceGenome | HGNC:42693 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000563710.7 | hg38 | chr13 | 51,082,119 | 51,111,274 | 29,156 |
ENST00000563710.7 | hg19 | chr13 | 51,656,255 | 51,685,410 | 29,156 |
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