RABAC1 Rab acceptor 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 1 | 0 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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14 |
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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 |
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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 | PRA1 |
SYNONYM | PRAF1 |
SYNONYM | YIP3 |
MIM | 604925 OMIM |
HGNC | HGNC:9794 HGNC |
Ensembl | ENSG00000105404 Ensembl |
AllianceGenome | HGNC:9794 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000601891.5 | hg38 | chr19 | 41,956,681 | 41,959,299 | 2,619 |
ENST00000222008.11 | hg38 | chr19 | 41,956,683 | 41,959,321 | 2,639 |
ENST00000601078.5 | hg38 | chr19 | 41,956,781 | 41,959,275 | 2,495 |
ENST00000601891.5 | hg19 | chr19 | 42,460,833 | 42,463,451 | 2,619 |
ENST00000222008.11 | hg19 | chr19 | 42,460,835 | 42,463,473 | 2,639 |
ENST00000601078.5 | hg19 | chr19 | 42,460,933 | 42,463,427 | 2,495 |
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