RAB35 RAB35, member RAS oncogene family
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 10 | 0 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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2 |
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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 |
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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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SYNONYM | H-ray |
SYNONYM | RAB1C |
SYNONYM | RAY |
MIM | 604199 OMIM |
HGNC | HGNC:9774 HGNC |
Ensembl | ENSG00000111737 Ensembl |
AllianceGenome | HGNC:9774 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000229340.10 | hg38 | chr12 | 120,095,099 | 120,116,753 | 21,655 |
ENST00000534951.5 | hg38 | chr12 | 120,096,904 | 120,116,767 | 19,864 |
ENST00000229340.10 | hg19 | chr12 | 120,532,903 | 120,554,557 | 21,655 |
ENST00000534951.5 | hg19 | chr12 | 120,534,708 | 120,554,571 | 19,864 |
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