LOC100996437 uncharacterized LOC100996437
Information
- Symbol
- LOC100996437
- Type
- ncRNA
- Description
- uncharacterized LOC100996437
- Entrez Gene ID
- 100996437
- Genome
- hg19
- Position
- chr7:66,134,341-66,136,510
- Genome
- hg38
- Position
- chr7:66,669,354-66,671,523
- Ensembl
- ENSG00000226824 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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Category | : |
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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 | ENSG00000226824 Ensembl |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000657342.1 | hg38 | chr7 | 66,654,578 | 66,670,413 | 15,836 |
ENST00000448096.1 | hg38 | chr7 | 66,654,538 | 66,666,299 | 11,762 |
ENST00000662347.1 | hg38 | chr7 | 66,669,354 | 66,671,523 | 2,170 |
ENST00000448096.1 | hg19 | chr7 | 66,119,525 | 66,131,286 | 11,762 |
ENST00000657342.1 | hg19 | chr7 | 66,119,565 | 66,135,400 | 15,836 |
ENST00000662347.1 | hg19 | chr7 | 66,134,341 | 66,136,510 | 2,170 |
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