LINC02210-CRHR1 LINC02210-CRHR1 readthrough
Information
- Symbol
- LINC02210-CRHR1
- Type
- protein-coding
- Description
- LINC02210-CRHR1 readthrough
- Entrez Gene ID
- 104909134
- Genome
- hg19
- Position
- chr17:43,697,710-43,913,192
- Genome
- hg38
- Position
- chr17:45,620,344-45,835,826
- HGNC
- HGNC:51483 HGNC
- Ensembl
- ENSG00000263715 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Likely benign | 0 | 10 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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52 |
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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 |
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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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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 | CRHR1-IT1-CRHR1 |
SYNONYM | MGC57346-CRHR1 |
HGNC | HGNC:51483 HGNC |
Ensembl | ENSG00000263715 Ensembl |
AllianceGenome | HGNC:51483 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000634540.1 | hg38 | chr17 | 45,620,344 | 45,835,826 | 215,483 |
ENST00000634540.1 | hg19 | chr17 | 43,697,710 | 43,913,192 | 215,483 |
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