RANBP3 RAN binding protein 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 62 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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64 |
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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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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000439268.6 | hg38 | chr19 | 5,916,139 | 5,978,108 | 61,970 |
ENST00000034275.12 | hg38 | chr19 | 5,917,352 | 5,978,086 | 60,735 |
ENST00000591092.5 | hg38 | chr19 | 5,917,323 | 5,978,093 | 60,771 |
ENST00000340578.10 | hg38 | chr19 | 5,916,139 | 5,978,140 | 62,002 |
ENST00000340578.10 | hg19 | chr19 | 5,916,150 | 5,978,151 | 62,002 |
ENST00000034275.12 | hg19 | chr19 | 5,917,363 | 5,978,097 | 60,735 |
ENST00000439268.6 | hg19 | chr19 | 5,916,150 | 5,978,119 | 61,970 |
ENST00000591092.5 | hg19 | chr19 | 5,917,334 | 5,978,104 | 60,771 |
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