LINC00664 long intergenic non-protein coding RNA 664
Information
- Symbol
- LINC00664
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 664
- Entrez Gene ID
- 400680
- Genome
- hg19
- Position
- chr19:21,666,517-21,686,040
- Genome
- hg38
- Position
- chr19:21,483,715-21,503,238
- HGNC
- HGNC:44319 HGNC
- Ensembl
- ENSG00000268658 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 |
---|---|---|---|---|---|
ENST00000599078.1 | hg38 | chr19 | 21,483,715 | 21,503,238 | 19,524 |
ENST00000596718.5 | hg38 | chr19 | 21,483,374 | 21,499,298 | 15,925 |
ENST00000596203.1 | hg38 | chr19 | 21,494,285 | 21,499,893 | 5,609 |
ENST00000596718.5 | hg19 | chr19 | 21,666,176 | 21,682,100 | 15,925 |
ENST00000599078.1 | hg19 | chr19 | 21,666,517 | 21,686,040 | 19,524 |
ENST00000596203.1 | hg19 | chr19 | 21,677,087 | 21,682,695 | 5,609 |
Genome browser