ARL1 ADP ribosylation factor like GTPase 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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4 |
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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.]
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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 |
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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | ARFL1 |
MIM | 603425 OMIM |
HGNC | HGNC:692 HGNC |
Ensembl | ENSG00000120805 Ensembl |
AllianceGenome | HGNC:692 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000551671.5 | hg38 | chr12 | 101,396,143 | 101,407,753 | 11,611 |
ENST00000539055.5 | hg38 | chr12 | 101,394,918 | 101,407,746 | 12,829 |
ENST00000551688.1 | hg38 | chr12 | 101,395,488 | 101,407,749 | 12,262 |
ENST00000551828.5 | hg38 | chr12 | 101,395,592 | 101,407,463 | 11,872 |
ENST00000261636.13 | hg38 | chr12 | 101,393,116 | 101,407,772 | 14,657 |
ENST00000536227.5 | hg38 | chr12 | 101,394,944 | 101,407,461 | 12,518 |
ENST00000261636.13 | hg19 | chr12 | 101,786,894 | 101,801,550 | 14,657 |
ENST00000539055.5 | hg19 | chr12 | 101,788,696 | 101,801,524 | 12,829 |
ENST00000536227.5 | hg19 | chr12 | 101,788,722 | 101,801,239 | 12,518 |
ENST00000551688.1 | hg19 | chr12 | 101,789,266 | 101,801,527 | 12,262 |
ENST00000551828.5 | hg19 | chr12 | 101,789,370 | 101,801,241 | 11,872 |
ENST00000551671.5 | hg19 | chr12 | 101,789,921 | 101,801,531 | 11,611 |
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