ARHGAP33 Rho GTPase activating protein 33

Information
Symbol
ARHGAP33
Type
protein-coding
Description
Rho GTPase activating protein 33
Entrez Gene ID
115703
Genome
hg19
Position
chr19:36,266,466-36,279,724
Genome
hg38
Position
chr19:35,775,564-35,788,822
MIM
614902 OMIM
HGNC
HGNC:23085 HGNC
Ensembl
ENSG00000004777 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 16
Uncertain significance 0 134
Ranking
ClinVar
0
0
0
158
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 :
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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 NOMA-GAP
SYNONYM SNX26
SYNONYM TCGAP
MIM 614902 OMIM
HGNC HGNC:23085 HGNC
Ensembl ENSG00000004777 Ensembl
AllianceGenome HGNC:23085
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000314737.9 hg38 chr19 35,775,575 35,788,822 13,248
ENST00000007510.9 hg38 chr19 35,775,564 35,788,822 13,259
ENST00000378944.9 hg38 chr19 35,775,515 35,788,822 13,308
ENST00000378944.9 hg19 chr19 36,266,417 36,279,724 13,308
ENST00000007510.9 hg19 chr19 36,266,466 36,279,724 13,259
ENST00000314737.9 hg19 chr19 36,266,477 36,279,724 13,248
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