LINC01449 long intergenic non-protein coding RNA 1449
Information
- Symbol
- LINC01449
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 1449
- Entrez Gene ID
- 101928773
- Genome
- hg19
- Position
- chr7:41,141,202-41,173,105
- Genome
- hg38
- Position
- chr7:41,101,604-41,133,507
- HGNC
- HGNC:50791 HGNC
- Ensembl
- ENSG00000224017 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 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000667448.1 | hg38 | chr7 | 41,097,493 | 41,108,871 | 11,379 |
ENST00000440213.1 | hg38 | chr7 | 41,101,604 | 41,133,507 | 31,904 |
ENST00000667448.1 | hg19 | chr7 | 41,137,091 | 41,148,469 | 11,379 |
ENST00000440213.1 | hg19 | chr7 | 41,141,202 | 41,173,105 | 31,904 |
Genome browser