RNF112 ring finger protein 112

Information
Symbol
RNF112
Type
protein-coding
Description
ring finger protein 112
Entrez Gene ID
7732
Genome
hg19
Position
chr17:19,314,545-19,320,589
Genome
hg38
Position
chr17:19,411,232-19,417,276
MIM
601237 OMIM
HGNC
HGNC:12968 HGNC
Ensembl
ENSG00000128482 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 4
not provided 2 0
Uncertain significance 0 58
Ranking
ClinVar
0
0
0
66
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
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 BFP
SYNONYM ZNF179
MIM 601237 OMIM
HGNC HGNC:12968 HGNC
Ensembl ENSG00000128482 Ensembl
AllianceGenome HGNC:12968
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000461366.2 hg38 chr17 19,411,232 19,417,276 6,045
ENST00000461366.2 hg19 chr17 19,314,545 19,320,589 6,045
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