LOC100506606 uncharacterized LOC100506606
Information
- Symbol
- LOC100506606
- Type
- ncRNA
- Description
- uncharacterized LOC100506606
- Entrez Gene ID
- 100506606
- Genome
- hg19
- Position
- chr12:29,430,888-29,436,184
- Genome
- hg38
- Position
- chr12:29,277,955-29,283,251
- Ensembl
- ENSG00000257176 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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0 |
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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 |
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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Ensembl | ENSG00000257176 Ensembl |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000553105.1 | hg38 | chr12 | 29,280,418 | 29,317,848 | 37,431 |
ENST00000655500.1 | hg38 | chr12 | 29,277,955 | 29,283,251 | 5,297 |
ENST00000655500.1 | hg19 | chr12 | 29,430,888 | 29,436,184 | 5,297 |
ENST00000553105.1 | hg19 | chr12 | 29,433,351 | 29,470,781 | 37,431 |
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