GPATCH1 G-patch domain containing 1

Information
Symbol
GPATCH1
Type
protein-coding
Description
G-patch domain containing 1
Entrez Gene ID
55094
Genome
hg19
Position
chr19:33,572,087-33,621,448
Genome
hg38
Position
chr19:33,081,181-33,130,542
HGNC
HGNC:24658 HGNC
Ensembl
ENSG00000076650 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 4
Uncertain significance 0 108
Ranking
ClinVar
0
0
0
116
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
SYNONYM ECGP
SYNONYM GPATC1
HGNC HGNC:24658 HGNC
Ensembl ENSG00000076650 Ensembl
AllianceGenome HGNC:24658
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000170564.7 hg38 chr19 33,081,181 33,130,542 49,362
ENST00000170564.7 hg19 chr19 33,572,087 33,621,448 49,362
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