ARHGAP23 Rho GTPase activating protein 23

Information
Symbol
ARHGAP23
Type
protein-coding
Description
Rho GTPase activating protein 23
Entrez Gene ID
57636
Genome
hg19
Position
chr17:36,584,708-36,668,621
Genome
hg38
Position
chr17:38,428,464-38,512,385
MIM
610590 OMIM
HGNC
HGNC:29293 HGNC
Ensembl
ENSG00000275832 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
Uncertain significance 0 248
Ranking
ClinVar
0
0
0
256
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
MIM 610590 OMIM
HGNC HGNC:29293 HGNC
Ensembl ENSG00000275832 Ensembl
AllianceGenome HGNC:29293
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000620417.4 hg38 chr17 38,428,486 38,510,136 81,651
ENST00000616767.2 hg38 chr17 38,453,690 38,512,385 58,696
ENST00000622683.5 hg38 chr17 38,428,464 38,512,385 83,922
ENST00000633445.2 hg38 chr17 38,419,280 38,512,385 93,106
ENST00000633445.2 hg19 chr17 36,575,523 36,668,621 93,099
ENST00000622683.5 hg19 chr17 36,584,708 36,668,621 83,914
ENST00000620417.4 hg19 chr17 36,584,730 36,666,372 81,643
ENST00000616767.2 hg19 chr17 36,609,934 36,668,621 58,688
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