FAM66C family with sequence similarity 66 member C
Information
- Symbol
- FAM66C
- Type
- ncRNA
- Description
- family with sequence similarity 66 member C
- Entrez Gene ID
- 440078
- Genome
- hg19
- Position
- chr12:8,332,818-8,353,596
- Genome
- hg38
- Position
- chr12:8,180,222-8,201,000
- HGNC
- HGNC:21644 HGNC
- Ensembl
- ENSG00000226711 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
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
[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 | |||||
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| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
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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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| 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 |
|---|---|---|---|---|---|
| ENST00000541558.5 | hg38 | chr12 | 8,180,269 | 8,199,881 | 19,613 |
| ENST00000456135.6 | hg38 | chr12 | 8,180,209 | 8,204,386 | 24,178 |
| ENST00000685711.1 | hg38 | chr12 | 8,180,260 | 8,183,128 | 2,869 |
| ENST00000535567.5 | hg38 | chr12 | 8,193,531 | 8,204,128 | 10,598 |
| ENST00000653230.1 | hg38 | chr12 | 8,193,573 | 8,200,966 | 7,394 |
| ENST00000372173.5 | hg38 | chr12 | 8,188,485 | 8,216,035 | 27,551 |
| ENST00000544214.5 | hg38 | chr12 | 8,180,222 | 8,201,000 | 20,779 |
| ENST00000456135.6 | hg19 | chr12 | 8,332,805 | 8,356,982 | 24,178 |
| ENST00000544214.5 | hg19 | chr12 | 8,332,818 | 8,353,596 | 20,779 |
| ENST00000685711.1 | hg19 | chr12 | 8,332,856 | 8,335,724 | 2,869 |
| ENST00000541558.5 | hg19 | chr12 | 8,332,865 | 8,352,477 | 19,613 |
| ENST00000372173.5 | hg19 | chr12 | 8,341,081 | 8,368,631 | 27,551 |
| ENST00000535567.5 | hg19 | chr12 | 8,346,127 | 8,356,724 | 10,598 |
| ENST00000653230.1 | hg19 | chr12 | 8,346,169 | 8,353,562 | 7,394 |
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