ARAF A-Raf proto-oncogene, serine/threonine kinase
Information
- Symbol
- ARAF
- Type
- protein-coding
- Description
- A-Raf proto-oncogene, serine/threonine kinase
- Entrez Gene ID
- 369
- Genome
- hg19
- Position
- chrX:47,420,604-47,431,307
- Genome
- hg38
- Position
- chrX:47,561,205-47,571,908
- MIM
- 311010 OMIM
- HGNC
- HGNC:646 HGNC
- Ensembl
- ENSG00000078061 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely pathogenic | 0 | 6 |
| Benign | 0 | 6 |
| Likely benign | 0 | 4 |
| not provided | 72 | 0 |
| Uncertain significance | 0 | 44 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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54 |
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6 |
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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| 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 | A-RAF |
| SYNONYM | ARAF1 |
| SYNONYM | PKS2 |
| SYNONYM | RAFA1 |
| MIM | 311010 OMIM |
| HGNC | HGNC:646 HGNC |
| Ensembl | ENSG00000078061 Ensembl |
| AllianceGenome | HGNC:646 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000377039.2 | hg38 | chrX | 47,561,222 | 47,565,975 | 4,754 |
| ENST00000377045.9 | hg38 | chrX | 47,561,205 | 47,571,908 | 10,704 |
| ENST00000377045.9 | hg19 | chrX | 47,420,604 | 47,431,307 | 10,704 |
| ENST00000377039.2 | hg19 | chrX | 47,420,621 | 47,425,374 | 4,754 |
| Key | Value |
|---|---|
| strand | + |
| UniProt | OG |
| start | 47,420,498 |
| Gene Symbol | ARAF |
| Entrez GeneId | 369 |
| Chr Band | Xp11.4-p11.2 |
| end | 47,431,319 |
| chr | chrX |
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