C1orf35 chromosome 1 open reading frame 35
Information
- Symbol
- C1orf35
- Type
- protein-coding
- Description
- chromosome 1 open reading frame 35
- Entrez Gene ID
- 79169
- Genome
- hg19
- Position
- chr1:228,288,432-228,291,026
- Genome
- hg38
- Position
- chr1:228,100,731-228,103,325
- HGNC
- HGNC:19032 HGNC
- Ensembl
- ENSG00000143793 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
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
[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 |
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 |
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SYNONYM | MMTAG2 |
HGNC | HGNC:19032 HGNC |
Ensembl | ENSG00000143793 Ensembl |
AllianceGenome | HGNC:19032 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000272139.5 | hg38 | chr1 | 228,100,731 | 228,103,325 | 2,595 |
ENST00000272139.5 | hg19 | chr1 | 228,288,432 | 228,291,026 | 2,595 |
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