ARL4A ADP ribosylation factor like GTPase 4A
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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8 |
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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
Search Word
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 |
Search Word
Target data | : |
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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Category | : |
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Search word | : | |
Filtering | : |
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 | ARL4 |
MIM | 604786 OMIM |
HGNC | HGNC:695 HGNC |
Ensembl | ENSG00000122644 Ensembl |
AllianceGenome | HGNC:695 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000396664.2 | hg38 | chr7 | 12,686,908 | 12,689,176 | 2,269 |
ENST00000396663.2 | hg38 | chr7 | 12,687,286 | 12,690,934 | 3,649 |
ENST00000396662.5 | hg38 | chr7 | 12,686,856 | 12,689,179 | 2,324 |
ENST00000651779.1 | hg38 | chr7 | 12,687,633 | 12,690,958 | 3,326 |
ENST00000404894.1 | hg38 | chr7 | 12,687,635 | 12,688,914 | 1,280 |
ENST00000356797.7 | hg38 | chr7 | 12,686,908 | 12,689,176 | 2,269 |
ENST00000396662.5 | hg19 | chr7 | 12,726,481 | 12,728,804 | 2,324 |
ENST00000356797.7 | hg19 | chr7 | 12,726,533 | 12,728,801 | 2,269 |
ENST00000396664.2 | hg19 | chr7 | 12,726,533 | 12,728,801 | 2,269 |
ENST00000396663.2 | hg19 | chr7 | 12,726,911 | 12,730,559 | 3,649 |
ENST00000651779.1 | hg19 | chr7 | 12,727,258 | 12,730,583 | 3,326 |
ENST00000404894.1 | hg19 | chr7 | 12,727,260 | 12,728,539 | 1,280 |
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