SLC7A14-AS1 SLC7A14 antisense RNA 1
Information
- Symbol
- SLC7A14-AS1
- Type
- ncRNA
- Description
- SLC7A14 antisense RNA 1
- Entrez Gene ID
- 101928583
- Genome
- hg19
- Position
- chr3:170,185,091-170,195,669
- Genome
- hg38
- Position
- chr3:170,467,303-170,477,881
- HGNC
- HGNC:54092 HGNC
- Ensembl
- ENSG00000285051 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely pathogenic | 1 | 0 |
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
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| 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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000661313.1 | hg38 | chr3 | 170,467,303 | 170,477,881 | 10,579 |
| ENST00000480067.1 | hg38 | chr3 | 170,467,282 | 170,755,208 | 287,927 |
| ENST00000663245.1 | hg38 | chr3 | 170,467,247 | 170,605,980 | 138,734 |
| ENST00000643719.1 | hg38 | chr3 | 170,448,639 | 170,671,497 | 222,859 |
| ENST00000643719.1 | hg19 | chr3 | 170,166,427 | 170,389,286 | 222,860 |
| ENST00000663245.1 | hg19 | chr3 | 170,185,035 | 170,323,769 | 138,735 |
| ENST00000480067.1 | hg19 | chr3 | 170,185,070 | 170,472,997 | 287,928 |
| ENST00000661313.1 | hg19 | chr3 | 170,185,091 | 170,195,669 | 10,579 |
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