LOC105375523 uncharacterized LOC105375523
Information
- Symbol
- LOC105375523
- Type
- ncRNA
- Description
- uncharacterized LOC105375523
- Entrez Gene ID
- 105375523
- Genome
- hg19
- Position
- chr7:135,777,673-135,928,459
- Genome
- hg38
- Position
- chr7:136,092,925-136,243,711
- Ensembl
- ENSG00000232053 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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 | ENSG00000232053 Ensembl |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000656605.1 | hg38 | chr7 | 136,405,207 | 136,437,447 | 32,241 |
ENST00000445293.6 | hg38 | chr7 | 136,092,925 | 136,437,163 | 344,239 |
ENST00000670875.1 | hg38 | chr7 | 136,304,411 | 136,437,444 | 133,034 |
ENST00000668062.1 | hg38 | chr7 | 136,092,923 | 136,437,785 | 344,863 |
ENST00000437569.1 | hg38 | chr7 | 136,405,263 | 136,437,382 | 32,120 |
ENST00000435996.1 | hg38 | chr7 | 136,092,957 | 136,437,426 | 344,470 |
ENST00000659747.1 | hg38 | chr7 | 136,092,925 | 136,243,711 | 150,787 |
ENST00000454735.1 | hg38 | chr7 | 136,427,395 | 136,437,410 | 10,016 |
ENST00000657456.1 | hg38 | chr7 | 136,092,913 | 136,437,407 | 344,495 |
ENST00000657456.1 | hg19 | chr7 | 135,777,661 | 136,122,155 | 344,495 |
ENST00000668062.1 | hg19 | chr7 | 135,777,671 | 136,122,533 | 344,863 |
ENST00000659747.1 | hg19 | chr7 | 135,777,673 | 135,928,459 | 150,787 |
ENST00000445293.6 | hg19 | chr7 | 135,777,673 | 136,121,911 | 344,239 |
ENST00000435996.1 | hg19 | chr7 | 135,777,705 | 136,122,174 | 344,470 |
ENST00000670875.1 | hg19 | chr7 | 135,989,159 | 136,122,192 | 133,034 |
ENST00000656605.1 | hg19 | chr7 | 136,089,955 | 136,122,195 | 32,241 |
ENST00000437569.1 | hg19 | chr7 | 136,090,011 | 136,122,130 | 32,120 |
ENST00000454735.1 | hg19 | chr7 | 136,112,143 | 136,122,158 | 10,016 |
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