RAB15 RAB15, member RAS oncogene family
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 12 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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16 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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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| 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 |
|---|---|
| MIM | 619547 OMIM |
| HGNC | HGNC:20150 HGNC |
| Ensembl | ENSG00000139998 Ensembl |
| AllianceGenome | HGNC:20150 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000267512.9 | hg38 | chr14 | 64,945,814 | 64,972,157 | 26,344 |
| ENST00000646728.1 | hg38 | chr14 | 64,945,839 | 64,972,760 | 26,922 |
| ENST00000646754.1 | hg38 | chr14 | 64,945,827 | 64,972,935 | 27,109 |
| ENST00000426039.8 | hg38 | chr14 | 64,945,827 | 64,972,778 | 26,952 |
| ENST00000533601.7 | hg38 | chr14 | 64,945,816 | 64,972,336 | 26,521 |
| ENST00000554593.2 | hg38 | chr14 | 64,945,827 | 64,972,776 | 26,950 |
| ENST00000267512.9 | hg19 | chr14 | 65,412,532 | 65,438,875 | 26,344 |
| ENST00000533601.7 | hg19 | chr14 | 65,412,534 | 65,439,054 | 26,521 |
| ENST00000554593.2 | hg19 | chr14 | 65,412,545 | 65,439,494 | 26,950 |
| ENST00000426039.8 | hg19 | chr14 | 65,412,545 | 65,439,496 | 26,952 |
| ENST00000646754.1 | hg19 | chr14 | 65,412,545 | 65,439,653 | 27,109 |
| ENST00000646728.1 | hg19 | chr14 | 65,412,557 | 65,439,478 | 26,922 |
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