ARHGAP44 Rho GTPase activating protein 44

Information
Symbol
ARHGAP44
Type
protein-coding
Description
Rho GTPase activating protein 44
Entrez Gene ID
9912
Genome
hg19
Position
chr17:12,692,815-12,894,960
Genome
hg38
Position
chr17:12,789,498-12,991,643
MIM
617716 OMIM
HGNC
HGNC:29096 HGNC
Ensembl
ENSG00000006740 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 10
Uncertain significance 0 74
Ranking
ClinVar
0
0
0
86
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 :
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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 NPC-A-10
SYNONYM RICH2
MIM 617716 OMIM
HGNC HGNC:29096 HGNC
Ensembl ENSG00000006740 Ensembl
AllianceGenome HGNC:29096
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000262444.13 hg38 chr17 12,789,760 12,990,584 200,825
ENST00000379672.10 hg38 chr17 12,789,498 12,991,643 202,146
ENST00000340825.7 hg38 chr17 12,789,539 12,991,643 202,105
ENST00000379672.10 hg19 chr17 12,692,815 12,894,960 202,146
ENST00000340825.7 hg19 chr17 12,692,856 12,894,960 202,105
ENST00000262444.13 hg19 chr17 12,693,077 12,893,901 200,825
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