FBXW10B F-box and WD repeat domain containing 10B
Information
- Symbol
- FBXW10B
- Type
- protein-coding
- Description
- F-box and WD repeat domain containing 10B
- Entrez Gene ID
- 374286
- Genome
- hg19
- Position
- chr17:15,491,977-15,522,826
- Genome
- hg38
- Position
- chr17:15,583,886-15,619,704
- MIM
- 604596 OMIM
- HGNC
- HGNC:14379 HGNC
- Ensembl
- ENSG00000241322 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 10 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
16 |
 |
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
|
| 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 | C170RF1 |
| SYNONYM | C17ORF1 |
| SYNONYM | C17ORF1A |
| SYNONYM | CDRT1 |
| SYNONYM | FBXW10P1 |
| SYNONYM | HREP |
| SYNONYM | SM25H2 |
| MIM | 604596 OMIM |
| HGNC | HGNC:14379 HGNC |
| Ensembl | ENSG00000241322 Ensembl |
| AllianceGenome | HGNC:14379 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000354433.7 | hg38 | chr17 | 15,588,388 | 15,598,797 | 10,410 |
| ENST00000583965.5 | hg38 | chr17 | 15,588,902 | 15,598,618 | 9,717 |
| ENST00000630868.1 | hg38 | chr17 | 15,565,483 | 15,566,276 | 794 |
| ENST00000395906.8 | hg38 | chr17 | 15,583,886 | 15,619,704 | 35,819 |
| ENST00000395667.7 | hg38 | chr17 | 15,565,484 | 15,619,512 | 54,029 |
| ENST00000354433.3 | hg19 | chr17 | 15,491,702 | 15,502,111 | 10,410 |
| ENST00000395906.3 | hg19 | chr17 | 15,491,977 | 15,522,826 | 30,850 |
| ENST00000583965.1 | hg19 | chr17 | 15,492,216 | 15,501,932 | 9,717 |
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