FAM181A-AS1 FAM181A antisense RNA 1
Information
- Symbol
- FAM181A-AS1
- Type
- ncRNA
- Description
- FAM181A antisense RNA 1
- Entrez Gene ID
- 283592
- Genome
- hg19
- Position
- chr14:94,371,076-94,392,718
- Genome
- hg38
- Position
- chr14:93,904,730-93,926,372
- HGNC
- HGNC:20133 HGNC
- Ensembl
- ENSG00000258584 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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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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| 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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| 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 | C14orf86 |
| HGNC | HGNC:20133 HGNC |
| Ensembl | ENSG00000258584 Ensembl |
| AllianceGenome | HGNC:20133 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000554538.1 | hg38 | chr14 | 93,923,673 | 93,926,966 | 3,294 |
| ENST00000555732.2 | hg38 | chr14 | 93,922,476 | 93,927,066 | 4,591 |
| ENST00000554742.1 | hg38 | chr14 | 93,904,730 | 93,926,372 | 21,643 |
| ENST00000556290.1 | hg38 | chr14 | 93,923,617 | 93,926,340 | 2,724 |
| ENST00000554742.1 | hg19 | chr14 | 94,371,076 | 94,392,718 | 21,643 |
| ENST00000555732.2 | hg19 | chr14 | 94,388,822 | 94,393,412 | 4,591 |
| ENST00000556290.1 | hg19 | chr14 | 94,389,963 | 94,392,686 | 2,724 |
| ENST00000554538.1 | hg19 | chr14 | 94,390,019 | 94,393,312 | 3,294 |
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