FAM66B family with sequence similarity 66 member B
Information
- Symbol
- FAM66B
- Type
- ncRNA
- Description
- family with sequence similarity 66 member B
- Entrez Gene ID
- 100128890
- Genome
- hg19
- Position
- chr8:7,156,266-7,212,856
- Genome
- hg38
- Position
- chr8:7,298,744-7,355,334
- HGNC
- HGNC:28890 HGNC
- Ensembl
- ENSG00000215374 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 1 | 0 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
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0 |
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0 |
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0 |
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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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| 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 | FAM66E |
| HGNC | HGNC:28890 HGNC |
| Ensembl | ENSG00000215374 Ensembl |
| AllianceGenome | HGNC:28890 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000663272.1 | hg38 | chr8 | 7,298,744 | 7,355,334 | 56,591 |
| ENST00000606573.1 | hg38 | chr8 | 7,318,540 | 7,355,339 | 36,800 |
| ENST00000663272.1 | hg19 | chr8 | 7,156,266 | 7,212,856 | 56,591 |
| ENST00000606573.1 | hg19 | chr8 | 7,176,062 | 7,212,861 | 36,800 |
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