ARFGAP1 ADP ribosylation factor GTPase activating protein 1
Information
- Symbol
- ARFGAP1
- Type
- protein-coding
- Description
- ADP ribosylation factor GTPase activating protein 1
- Entrez Gene ID
- 55738
- Genome
- hg19
- Position
- chr20:61,904,217-61,920,696
- Genome
- hg38
- Position
- chr20:63,272,865-63,289,344
- MIM
- 608377 OMIM
- HGNC
- HGNC:15852 HGNC
- Ensembl
- ENSG00000101199 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 66 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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74 |
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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 |
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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 |
---|---|
SYNONYM | ARF1GAP |
SYNONYM | HRIHFB2281 |
MIM | 608377 OMIM |
HGNC | HGNC:15852 HGNC |
Ensembl | ENSG00000101199 Ensembl |
AllianceGenome | HGNC:15852 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000519604.5 | hg38 | chr20 | 63,272,785 | 63,289,789 | 17,005 |
ENST00000547204.5 | hg38 | chr20 | 63,272,797 | 63,287,937 | 15,141 |
ENST00000353546.7 | hg38 | chr20 | 63,272,865 | 63,289,344 | 16,480 |
ENST00000370275.8 | hg38 | chr20 | 63,272,833 | 63,289,788 | 16,956 |
ENST00000519273.6 | hg38 | chr20 | 63,272,785 | 63,289,789 | 17,005 |
ENST00000370283.9 | hg38 | chr20 | 63,272,813 | 63,289,790 | 16,978 |
ENST00000519604.5 | hg19 | chr20 | 61,904,137 | 61,921,141 | 17,005 |
ENST00000353546.7 | hg19 | chr20 | 61,904,217 | 61,920,696 | 16,480 |
ENST00000370275.8 | hg19 | chr20 | 61,904,185 | 61,921,140 | 16,956 |
ENST00000370283.9 | hg19 | chr20 | 61,904,165 | 61,921,142 | 16,978 |
ENST00000519273.6 | hg19 | chr20 | 61,904,137 | 61,921,141 | 17,005 |
ENST00000547204.5 | hg19 | chr20 | 61,904,149 | 61,919,289 | 15,141 |
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