PRR5-ARHGAP8 PRR5-ARHGAP8 readthrough

Information
Symbol
PRR5-ARHGAP8
Type
protein-coding
Description
PRR5-ARHGAP8 readthrough
Entrez Gene ID
553158
Genome
hg19
Position
chr22:45,098,355-45,258,586
Genome
hg38
Position
chr22:44,702,475-44,862,706
HGNC
HGNC:34512 HGNC
Ensembl
ENSG00000248405 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 26
not provided 1 2
Uncertain significance 0 198
Ranking
ClinVar
0
0
0
230
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
HGNC HGNC:34512 HGNC
Ensembl ENSG00000248405 Ensembl
AllianceGenome HGNC:34512
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000352766.11 hg38 chr22 44,702,475 44,862,706 160,232
ENST00000361473.9 hg38 chr22 44,702,233 44,862,671 160,439
ENST00000361473.9 hg19 chr22 45,098,113 45,258,551 160,439
ENST00000352766.11 hg19 chr22 45,098,355 45,258,586 160,232
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