RACGAP1 Rac GTPase activating protein 1

Information
Symbol
RACGAP1
Type
protein-coding
Description
Rac GTPase activating protein 1
Entrez Gene ID
29127
Genome
hg19
Position
chr12:50,382,945-50,419,221
Genome
hg38
Position
chr12:49,989,162-50,025,438
MIM
604980 OMIM
HGNC
HGNC:9804 HGNC
Ensembl
ENSG00000161800 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Benign 0 28
Likely benign 0 2
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
76
6
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 CDAN3B
SYNONYM CYK4
SYNONYM HsCYK-4
SYNONYM ID-GAP
SYNONYM MgcRacGAP
MIM 604980 OMIM
HGNC HGNC:9804 HGNC
Ensembl ENSG00000161800 Ensembl
AllianceGenome HGNC:9804
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000312377.10 hg38 chr12 49,989,162 50,025,494 36,333
ENST00000551016.5 hg38 chr12 49,989,979 50,016,720 26,742
ENST00000454520.6 hg38 chr12 49,989,164 50,025,400 36,237
ENST00000427314.6 hg38 chr12 49,989,162 50,025,438 36,277
ENST00000547905.5 hg38 chr12 49,990,268 50,025,494 35,227
ENST00000548961.5 hg38 chr12 49,976,923 49,992,358 15,436
ENST00000427314.6 hg19 chr12 50,382,945 50,419,221 36,277
ENST00000312377.10 hg19 chr12 50,382,945 50,419,277 36,333
ENST00000454520.6 hg19 chr12 50,382,947 50,419,183 36,237
ENST00000548961.5 hg19 chr12 50,370,706 50,386,141 15,436
ENST00000547905.5 hg19 chr12 50,384,051 50,419,277 35,227
ENST00000551016.5 hg19 chr12 50,383,762 50,410,503 26,742
Genome browser