RAP2A RAP2A, member of RAS oncogene family
Information
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 2 |
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
[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 |
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | K-REV |
SYNONYM | KREV |
SYNONYM | RAP2 |
SYNONYM | RbBP-30 |
MIM | 179540 OMIM |
HGNC | HGNC:9861 HGNC |
Ensembl | ENSG00000125249 Ensembl |
AllianceGenome | HGNC:9861 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000245304.5 | hg38 | chr13 | 97,434,169 | 97,469,128 | 34,960 |
ENST00000245304.5 | hg19 | chr13 | 98,086,423 | 98,121,382 | 34,960 |
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