LOC105374524 uncharacterized LOC105374524
Information
- Symbol
- LOC105374524
- Type
- ncRNA
- Description
- uncharacterized LOC105374524
- Entrez Gene ID
- 105374524
- Genome
- hg19
- Position
- chr4:23,001,262-23,195,363
- Genome
- hg38
- Position
- chr4:22,999,639-23,193,740
- Ensembl
- ENSG00000248837 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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Category | : |
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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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Filtering | : |
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 | ENSG00000248837 Ensembl |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000654588.1 | hg38 | chr4 | 22,997,583 | 23,041,015 | 43,433 |
ENST00000506425.2 | hg38 | chr4 | 22,997,532 | 23,041,550 | 44,019 |
ENST00000655768.1 | hg38 | chr4 | 22,997,567 | 23,041,518 | 43,952 |
ENST00000667179.1 | hg38 | chr4 | 22,997,560 | 23,121,601 | 124,042 |
ENST00000653008.1 | hg38 | chr4 | 22,997,535 | 23,123,473 | 125,939 |
ENST00000666412.1 | hg38 | chr4 | 22,997,542 | 23,123,487 | 125,946 |
ENST00000663529.1 | hg38 | chr4 | 22,997,571 | 23,041,013 | 43,443 |
ENST00000660103.1 | hg38 | chr4 | 22,997,523 | 23,041,862 | 44,340 |
ENST00000654546.1 | hg38 | chr4 | 22,997,539 | 23,041,864 | 44,326 |
ENST00000658109.1 | hg38 | chr4 | 22,997,581 | 23,096,041 | 98,461 |
ENST00000663348.1 | hg38 | chr4 | 22,999,639 | 23,193,740 | 194,102 |
ENST00000511453.5 | hg38 | chr4 | 22,997,551 | 23,056,862 | 59,312 |
ENST00000654588.1 | hg19 | chr4 | 22,999,206 | 23,042,638 | 43,433 |
ENST00000511453.5 | hg19 | chr4 | 22,999,174 | 23,058,485 | 59,312 |
ENST00000506425.2 | hg19 | chr4 | 22,999,155 | 23,043,173 | 44,019 |
ENST00000653008.1 | hg19 | chr4 | 22,999,158 | 23,125,096 | 125,939 |
ENST00000654546.1 | hg19 | chr4 | 22,999,162 | 23,043,487 | 44,326 |
ENST00000655768.1 | hg19 | chr4 | 22,999,190 | 23,043,141 | 43,952 |
ENST00000663348.1 | hg19 | chr4 | 23,001,262 | 23,195,363 | 194,102 |
ENST00000658109.1 | hg19 | chr4 | 22,999,204 | 23,097,664 | 98,461 |
ENST00000660103.1 | hg19 | chr4 | 22,999,146 | 23,043,485 | 44,340 |
ENST00000663529.1 | hg19 | chr4 | 22,999,194 | 23,042,636 | 43,443 |
ENST00000666412.1 | hg19 | chr4 | 22,999,165 | 23,125,110 | 125,946 |
ENST00000667179.1 | hg19 | chr4 | 22,999,183 | 23,123,224 | 124,042 |
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