FAM167A-AS1 FAM167A antisense RNA 1
Information
- Symbol
- FAM167A-AS1
- Type
- ncRNA
- Description
- FAM167A antisense RNA 1
- Entrez Gene ID
- 83656
- Genome
- hg19
- Position
- chr8:11,251,633-11,296,167
- Genome
- hg38
- Position
- chr8:11,394,124-11,438,658
- HGNC
- HGNC:15548 HGNC
- Ensembl
- ENSG00000184608 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
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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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | C8orf12 |
| HGNC | HGNC:15548 HGNC |
| Ensembl | ENSG00000184608 Ensembl |
| AllianceGenome | HGNC:15548 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000624614.1 | hg38 | chr8 | 11,394,124 | 11,438,658 | 44,535 |
| ENST00000529305.5 | hg38 | chr8 | 11,390,424 | 11,435,001 | 44,578 |
| ENST00000533578.4 | hg38 | chr8 | 11,368,402 | 11,438,657 | 70,256 |
| ENST00000533578.4 | hg19 | chr8 | 11,225,911 | 11,296,166 | 70,256 |
| ENST00000529305.5 | hg19 | chr8 | 11,247,933 | 11,292,510 | 44,578 |
| ENST00000624614.1 | hg19 | chr8 | 11,251,633 | 11,296,167 | 44,535 |
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