ARHGAP11A Rho GTPase activating protein 11A

Information
Symbol
ARHGAP11A
Type
protein-coding
Description
Rho GTPase activating protein 11A
Entrez Gene ID
9824
Genome
hg19
Position
chr15:32,907,705-32,932,142
Genome
hg38
Position
chr15:32,615,504-32,639,941
MIM
610589 OMIM
HGNC
HGNC:15783 HGNC
Ensembl
ENSG00000198826 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Benign 0 16
Likely benign 0 12
Uncertain significance 0 84
Ranking
ClinVar
0
0
0
114
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
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM GAP (1-12)
MIM 610589 OMIM
HGNC HGNC:15783 HGNC
Ensembl ENSG00000198826 Ensembl
AllianceGenome HGNC:15783
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
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
Genome browser