RAB29 RAB29, member RAS oncogene family
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
not provided | 1 | 0 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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22 |
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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
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 |
Search Word
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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Search word | : | |
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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 | RAB7L |
SYNONYM | RAB7L1 |
MIM | 603949 OMIM |
HGNC | HGNC:9789 HGNC |
Ensembl | ENSG00000117280 Ensembl |
AllianceGenome | HGNC:9789 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000437324.6 | hg38 | chr1 | 205,769,703 | 205,775,451 | 5,749 |
ENST00000446390.6 | hg38 | chr1 | 205,769,718 | 205,775,233 | 5,516 |
ENST00000235932.8 | hg38 | chr1 | 205,769,437 | 205,775,449 | 6,013 |
ENST00000414729.1 | hg38 | chr1 | 205,770,300 | 205,775,459 | 5,160 |
ENST00000367139.8 | hg38 | chr1 | 205,767,986 | 205,775,482 | 7,497 |
ENST00000367139.8 | hg19 | chr1 | 205,737,114 | 205,744,610 | 7,497 |
ENST00000235932.8 | hg19 | chr1 | 205,738,565 | 205,744,577 | 6,013 |
ENST00000437324.6 | hg19 | chr1 | 205,738,831 | 205,744,579 | 5,749 |
ENST00000446390.6 | hg19 | chr1 | 205,738,846 | 205,744,361 | 5,516 |
ENST00000414729.1 | hg19 | chr1 | 205,739,428 | 205,744,587 | 5,160 |
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