LOC101928565 uncharacterized LOC101928565
Information
- Symbol
- LOC101928565
- Type
- ncRNA
- Description
- uncharacterized LOC101928565
- Entrez Gene ID
- 101928565
- Genome
- hg19
- Position
- chr1:168,370,067-168,391,894
- Genome
- hg38
- Position
- chr1:168,400,829-168,422,656
- Ensembl
- ENSG00000228697 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 | ENSG00000228697 Ensembl |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000702777.1 | hg38 | chr1 | 168,484,504 | 168,495,683 | 11,180 |
ENST00000636459.1 | hg38 | chr1 | 168,401,474 | 168,495,685 | 94,212 |
ENST00000702086.1 | hg38 | chr1 | 168,483,509 | 168,495,650 | 12,142 |
ENST00000422253.1 | hg38 | chr1 | 168,464,214 | 168,495,644 | 31,431 |
ENST00000686713.1 | hg38 | chr1 | 168,484,515 | 168,495,692 | 11,178 |
ENST00000441851.1 | hg38 | chr1 | 168,400,829 | 168,422,656 | 21,828 |
ENST00000650143.1 | hg38 | chr1 | 168,401,484 | 168,495,643 | 94,160 |
ENST00000655897.3 | hg38 | chr1 | 168,484,343 | 168,495,671 | 11,329 |
ENST00000441851.1 | hg19 | chr1 | 168,370,067 | 168,391,894 | 21,828 |
ENST00000636459.1 | hg19 | chr1 | 168,370,712 | 168,464,923 | 94,212 |
ENST00000650143.1 | hg19 | chr1 | 168,370,722 | 168,464,881 | 94,160 |
ENST00000422253.1 | hg19 | chr1 | 168,433,452 | 168,464,882 | 31,431 |
ENST00000655897.3 | hg19 | chr1 | 168,453,581 | 168,464,909 | 11,329 |
ENST00000702086.1 | hg19 | chr1 | 168,452,747 | 168,464,888 | 12,142 |
ENST00000702777.1 | hg19 | chr1 | 168,453,742 | 168,464,921 | 11,180 |
ENST00000686713.1 | hg19 | chr1 | 168,453,753 | 168,464,930 | 11,178 |
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