RAB39A RAB39A, member RAS oncogene family
Information
- Symbol
- RAB39A
- Type
- protein-coding
- Description
- RAB39A, member RAS oncogene family
- Entrez Gene ID
- 54734
- Genome
- hg19
- Position
- chr11:107,799,174-107,834,208
- Genome
- hg38
- Position
- chr11:107,928,448-107,963,482
- MIM
- 619558 OMIM
- HGNC
- HGNC:16521 HGNC
- Ensembl
- ENSG00000179331 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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6 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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MGeND data only
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | K28 |
SYNONYM | RAB39 |
MIM | 619558 OMIM |
HGNC | HGNC:16521 HGNC |
Ensembl | ENSG00000179331 Ensembl |
AllianceGenome | HGNC:16521 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000320578.3 | hg38 | chr11 | 107,928,448 | 107,963,482 | 35,035 |
ENST00000320578.3 | hg19 | chr11 | 107,799,174 | 107,834,208 | 35,035 |
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