ARHGAP11A Rho GTPase activating protein 11A
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Benign | 0 | 16 |
Likely benign | 0 | 12 |
Uncertain significance | 0 | 84 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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114 |
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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 | GAP (1-12) |
MIM | 610589 OMIM |
HGNC | HGNC:15783 HGNC |
Ensembl | ENSG00000198826 Ensembl |
AllianceGenome | HGNC:15783 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000543522.5 | hg38 | chr15 | 32,615,571 | 32,637,903 | 22,333 |
ENST00000567348.5 | hg38 | chr15 | 32,615,539 | 32,636,181 | 20,643 |
ENST00000563864.5 | hg38 | chr15 | 32,615,565 | 32,636,148 | 20,584 |
ENST00000565905.5 | hg38 | chr15 | 32,615,144 | 32,638,110 | 22,967 |
ENST00000361627.8 | hg38 | chr15 | 32,615,504 | 32,639,941 | 24,438 |
ENST00000565905.5 | hg19 | chr15 | 32,907,345 | 32,930,311 | 22,967 |
ENST00000361627.8 | hg19 | chr15 | 32,907,705 | 32,932,142 | 24,438 |
ENST00000567348.5 | hg19 | chr15 | 32,907,740 | 32,928,382 | 20,643 |
ENST00000563864.5 | hg19 | chr15 | 32,907,766 | 32,928,349 | 20,584 |
ENST00000543522.5 | hg19 | chr15 | 32,907,772 | 32,930,104 | 22,333 |
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