GIMAP1-GIMAP5 GIMAP1-GIMAP5 readthrough

Information
Symbol
GIMAP1-GIMAP5
Type
protein-coding
Description
GIMAP1-GIMAP5 readthrough
Entrez Gene ID
100527949
Genome
hg19
Position
chr7:150,413,756-150,440,734
Genome
hg38
Position
chr7:150,716,668-150,743,646
HGNC
HGNC:51257 HGNC
Ensembl
ENSG00000281887 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 6
Benign 0 6
Likely benign 0 6
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 32
Ranking
ClinVar
0
0
0
44
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
HGNC HGNC:51257 HGNC
Ensembl ENSG00000281887 Ensembl
AllianceGenome HGNC:51257
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000611999.4 hg38 chr7 150,716,668 150,743,646 26,979
ENST00000611999.4 hg19 chr7 150,413,756 150,440,734 26,979
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