RAB9A RAB9A, member RAS oncogene family
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
not provided | 7 | 0 |
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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20 |
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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
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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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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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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 | RAB9 |
MIM | 300284 OMIM |
HGNC | HGNC:9792 HGNC |
Ensembl | ENSG00000123595 Ensembl |
AllianceGenome | HGNC:9792 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000618931.2 | hg38 | chrX | 13,689,186 | 13,709,354 | 20,169 |
ENST00000464506.2 | hg38 | chrX | 13,689,128 | 13,710,504 | 21,377 |
ENST00000464506.2 | hg19 | chrX | 13,707,247 | 13,728,623 | 21,377 |
ENST00000618931.2 | hg19 | chrX | 13,707,305 | 13,727,473 | 20,169 |
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