C1orf131 chromosome 1 open reading frame 131
Information
- Symbol
- C1orf131
- Type
- protein-coding
- Description
- chromosome 1 open reading frame 131
- Entrez Gene ID
- 128061
- Genome
- hg19
- Position
- chr1:231,359,511-231,376,921
- Genome
- hg38
- Position
- chr1:231,223,765-231,241,175
- HGNC
- HGNC:25332 HGNC
- Ensembl
- ENSG00000143633 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
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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10 |
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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
[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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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000366649.7 | hg38 | chr1 | 231,223,765 | 231,241,175 | 17,411 |
ENST00000366651.7 | hg38 | chr1 | 231,223,763 | 231,241,178 | 17,416 |
ENST00000318906.6 | hg38 | chr1 | 231,223,763 | 231,241,170 | 17,408 |
ENST00000318906.6 | hg19 | chr1 | 231,359,509 | 231,376,916 | 17,408 |
ENST00000366651.7 | hg19 | chr1 | 231,359,509 | 231,376,924 | 17,416 |
ENST00000366649.7 | hg19 | chr1 | 231,359,511 | 231,376,921 | 17,411 |
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