NMI N-myc and STAT interactor

Information
Symbol
NMI
Type
protein-coding
Description
N-myc and STAT interactor
Entrez Gene ID
9111
Genome
hg19
Position
chr2:152,126,984-152,146,182
Genome
hg38
Position
chr2:151,270,470-151,289,668
MIM
603525 OMIM
HGNC
HGNC:7854 HGNC
Ensembl
ENSG00000123609 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
not provided 0 2
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
36
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
MIM 603525 OMIM
HGNC HGNC:7854 HGNC
Ensembl ENSG00000123609 Ensembl
AllianceGenome HGNC:7854
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000243346.10 hg38 chr2 151,270,470 151,289,668 19,199
ENST00000243346.10 hg19 chr2 152,126,984 152,146,182 19,199
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