ARHGAP11A-SCG5 ARHGAP11A-SCG5 readthrough

Information
Symbol
ARHGAP11A-SCG5
Type
protein-coding
Description
ARHGAP11A-SCG5 readthrough
Entrez Gene ID
114118903
Genome
hg19
Position
chr15:32,907,649-32,989,296
Genome
hg38
Position
chr15:32,615,448-32,697,095
HGNC
HGNC:56310 HGNC
Ensembl
ENSG00000288864 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Benign 0 48
Likely benign 0 44
Uncertain significance 0 90
Ranking
ClinVar
0
0
0
184
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
HGNC HGNC:56310 HGNC
Ensembl ENSG00000288864 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000692248.1 hg38 chr15 32,615,448 32,697,095 81,648
ENST00000689909.1 hg38 chr15 32,613,860 32,697,077 83,218
ENST00000689909.1 hg19 chr15 32,906,061 32,989,278 83,218
ENST00000692248.1 hg19 chr15 32,907,649 32,989,296 81,648
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