NIP7 nucleolar pre-rRNA processing protein NIP7

Information
Symbol
NIP7
Type
protein-coding
Description
nucleolar pre-rRNA processing protein NIP7
Entrez Gene ID
51388
Genome
hg19
Position
chr16:69,373,675-69,377,009
Genome
hg38
Position
chr16:69,339,772-69,343,106
MIM
619204 OMIM
HGNC
HGNC:24328 HGNC
Ensembl
ENSG00000132603 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 6
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
30
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 CGI-37
SYNONYM HSPC031
SYNONYM KD93
MIM 619204 OMIM
HGNC HGNC:24328 HGNC
Ensembl ENSG00000132603 Ensembl
AllianceGenome HGNC:24328
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000569637.6 hg38 chr16 69,339,568 69,340,887 1,320
ENST00000254941.6 hg38 chr16 69,339,797 69,343,104 3,308
ENST00000254940.10 hg38 chr16 69,339,772 69,343,106 3,335
ENST00000569637.6 hg19 chr16 69,373,471 69,374,790 1,320
ENST00000254940.10 hg19 chr16 69,373,675 69,377,009 3,335
ENST00000254941.6 hg19 chr16 69,373,700 69,377,007 3,308
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