ARHGAP42 Rho GTPase activating protein 42

Information
Symbol
ARHGAP42
Type
protein-coding
Description
Rho GTPase activating protein 42
Entrez Gene ID
143872
Genome
hg19
Position
chr11:100,558,019-100,864,672
Genome
hg38
Position
chr11:100,687,288-100,993,941
MIM
615936 OMIM
HGNC
HGNC:26545 HGNC
Ensembl
ENSG00000165895 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
not provided 1 0
Uncertain significance 0 84
Ranking
ClinVar
0
0
0
88
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
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 AD031
SYNONYM GRAF3
SYNONYM TMEM133
MIM 615936 OMIM
HGNC HGNC:26545 HGNC
Ensembl ENSG00000165895 Ensembl
AllianceGenome HGNC:26545
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000303130.4 hg38 chr11 100,992,080 100,993,934 1,855
ENST00000524892.7 hg38 chr11 100,687,653 100,993,941 306,289
ENST00000298815.13 hg38 chr11 100,687,288 100,993,941 306,654
ENST00000298815.13 hg19 chr11 100,558,019 100,864,672 306,654
ENST00000524892.7 hg19 chr11 100,558,384 100,864,672 306,289
ENST00000303130.4 hg19 chr11 100,862,811 100,864,665 1,855
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