RAB40B RAB40B, member RAS oncogene family
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| 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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44 |
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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 |
Prediction | |||||
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | RAR |
| SYNONYM | SEC4L |
| MIM | 619550 OMIM |
| HGNC | HGNC:18284 HGNC |
| Ensembl | ENSG00000141542 Ensembl |
| AllianceGenome | HGNC:18284 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000538809.6 | hg38 | chr17 | 82,657,911 | 82,698,662 | 40,752 |
| ENST00000571995.6 | hg38 | chr17 | 82,654,973 | 82,698,698 | 43,726 |
| ENST00000269347.10 | hg38 | chr17 | 82,657,067 | 82,698,687 | 41,621 |
| ENST00000571995.6 | hg19 | chr17 | 80,612,849 | 80,656,574 | 43,726 |
| ENST00000269347.10 | hg19 | chr17 | 80,614,943 | 80,656,563 | 41,621 |
| ENST00000538809.6 | hg19 | chr17 | 80,615,787 | 80,656,538 | 40,752 |
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