SLC12A9-AS1 SLC12A9 antisense RNA 1
Information
- Symbol
- SLC12A9-AS1
- Type
- ncRNA
- Description
- SLC12A9 antisense RNA 1
- Entrez Gene ID
- 105375430
- Genome
- hg19
- Position
- chr7:100,449,602-100,450,259
- Genome
- hg38
- Position
- chr7:100,851,980-100,852,637
- HGNC
- HGNC:40807 HGNC
- Ensembl
- ENSG00000236305 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 |
---|---|---|---|---|---|
ENST00000684935.1 | hg38 | chr7 | 100,851,980 | 100,852,637 | 658 |
ENST00000702979.1 | hg38 | chr7 | 100,851,980 | 100,852,637 | 658 |
ENST00000412754.2 | hg38 | chr7 | 100,837,314 | 100,852,635 | 15,322 |
ENST00000412754.2 | hg19 | chr7 | 100,434,936 | 100,450,257 | 15,322 |
ENST00000684935.1 | hg19 | chr7 | 100,449,602 | 100,450,259 | 658 |
ENST00000702979.1 | hg19 | chr7 | 100,449,602 | 100,450,259 | 658 |
Genome browser