IFNG interferon gamma

Information
Symbol
IFNG
Type
protein-coding
Description
interferon gamma
Entrez Gene ID
3458
Genome
hg19
Position
chr12:68,548,548-68,553,520
Genome
hg38
Position
chr12:68,154,768-68,159,740
MIM
147570 OMIM
HGNC
HGNC:5438 HGNC
Ensembl
ENSG00000111537 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 10
Likely benign 0 6
Conflicting classifications of pathogenicity 0 2
not provided 0 14
protective 0 2
Uncertain significance 0 32
Ranking
ClinVar
0
0
2
46
4
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 IFG
SYNONYM IFI
SYNONYM IMD69
MIM 147570 OMIM
HGNC HGNC:5438 HGNC
Ensembl ENSG00000111537 Ensembl
AllianceGenome HGNC:5438
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000229135.4 hg38 chr12 68,154,768 68,159,740 4,973
ENST00000229135.4 hg19 chr12 68,548,548 68,553,520 4,973
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