RAB37 RAB37, member RAS oncogene family
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 16 |
Uncertain significance | 0 | 68 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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84 |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
MGeND data only
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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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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MIM | 609956 OMIM |
HGNC | HGNC:30268 HGNC |
Ensembl | ENSG00000172794 Ensembl |
AllianceGenome | HGNC:30268 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000402449.8 | hg38 | chr17 | 74,671,141 | 74,745,874 | 74,734 |
ENST00000392613.10 | hg38 | chr17 | 74,737,256 | 74,747,335 | 10,080 |
ENST00000340415.7 | hg38 | chr17 | 74,670,578 | 74,747,334 | 76,757 |
ENST00000613645.1 | hg38 | chr17 | 74,737,271 | 74,747,334 | 10,064 |
ENST00000392610.5 | hg38 | chr17 | 74,737,232 | 74,747,335 | 10,104 |
ENST00000392615.9 | hg38 | chr17 | 74,736,820 | 74,747,300 | 10,481 |
ENST00000392614.8 | hg38 | chr17 | 74,736,917 | 74,747,335 | 10,419 |
ENST00000392612.7 | hg38 | chr17 | 74,737,230 | 74,747,335 | 10,106 |
ENST00000528438.5 | hg38 | chr17 | 74,736,598 | 74,746,192 | 9,595 |
ENST00000340415.7 | hg19 | chr17 | 72,666,717 | 72,743,473 | 76,757 |
ENST00000402449.8 | hg19 | chr17 | 72,667,280 | 72,742,013 | 74,734 |
ENST00000528438.5 | hg19 | chr17 | 72,732,737 | 72,742,331 | 9,595 |
ENST00000392615.9 | hg19 | chr17 | 72,732,959 | 72,743,439 | 10,481 |
ENST00000392614.8 | hg19 | chr17 | 72,733,056 | 72,743,474 | 10,419 |
ENST00000392612.7 | hg19 | chr17 | 72,733,369 | 72,743,474 | 10,106 |
ENST00000392610.5 | hg19 | chr17 | 72,733,371 | 72,743,474 | 10,104 |
ENST00000392613.10 | hg19 | chr17 | 72,733,395 | 72,743,474 | 10,080 |
ENST00000613645.1 | hg19 | chr17 | 72,733,410 | 72,743,473 | 10,064 |
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