ARF3 ADP ribosylation factor 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 8 |
Likely pathogenic | 0 | 4 |
Benign | 0 | 4 |
Conflicting classifications of pathogenicity | 0 | 2 |
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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18 |
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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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ENST00000541959.5 | hg38 | chr12 | 48,938,925 | 48,957,445 | 18,521 |
ENST00000447318.6 | hg38 | chr12 | 48,938,554 | 48,957,477 | 18,924 |
ENST00000256682.9 | hg38 | chr12 | 48,935,723 | 48,957,487 | 21,765 |
ENST00000256682.9 | hg19 | chr12 | 49,329,506 | 49,351,270 | 21,765 |
ENST00000447318.6 | hg19 | chr12 | 49,332,337 | 49,351,260 | 18,924 |
ENST00000541959.5 | hg19 | chr12 | 49,332,708 | 49,351,228 | 18,521 |
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