LOC101928438 uncharacterized LOC101928438
Information
- Symbol
- LOC101928438
- Type
- ncRNA
- Description
- uncharacterized LOC101928438
- Entrez Gene ID
- 101928438
- Genome
- hg19
- Position
- chr9:102,159,269-102,582,203
- Genome
- hg38
- Position
- chr9:99,396,987-99,819,921
- Ensembl
- ENSG00000237461 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
0 |
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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| Ensembl | ENSG00000237461 Ensembl |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000427039.1 | hg38 | chr9 | 99,585,786 | 99,819,889 | 234,104 |
| ENST00000652827.1 | hg38 | chr9 | 99,396,987 | 99,819,921 | 422,935 |
| ENST00000701763.1 | hg38 | chr9 | 99,717,544 | 99,819,895 | 102,352 |
| ENST00000652827.1 | hg19 | chr9 | 102,159,269 | 102,582,203 | 422,935 |
| ENST00000427039.1 | hg19 | chr9 | 102,348,068 | 102,582,171 | 234,104 |
| ENST00000701763.1 | hg19 | chr9 | 102,479,826 | 102,582,177 | 102,352 |
Genome browser




