EXOG exo/endonuclease G

Information
Symbol
EXOG
Type
protein-coding
Description
exo/endonuclease G
Entrez Gene ID
9941
Genome
hg19
Position
chr3:38,537,831-38,567,794
Genome
hg38
Position
chr3:38,496,340-38,526,303
MIM
604051 OMIM
HGNC
HGNC:3347 HGNC
Ensembl
ENSG00000157036 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 44
Ranking
ClinVar
0
0
0
46
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 ENDOGL1
SYNONYM ENDOGL2
SYNONYM ENGL
SYNONYM ENGL-a
SYNONYM ENGL-b
SYNONYM ENGLA
SYNONYM ENGLB
MIM 604051 OMIM
HGNC HGNC:3347 HGNC
Ensembl ENSG00000157036 Ensembl
AllianceGenome HGNC:3347
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000630638.1 hg38 chr3 38,496,342 38,496,850 509
ENST00000422077.6 hg38 chr3 38,496,345 38,524,699 28,355
ENST00000287675.10 hg38 chr3 38,496,340 38,526,303 29,964
ENST00000287675.10 hg19 chr3 38,537,831 38,567,794 29,964
ENST00000422077.6 hg19 chr3 38,537,836 38,566,190 28,355
ENST00000630638.1 hg19 chr3 38,537,833 38,538,341 509
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