RNF146 ring finger protein 146

Information
Symbol
RNF146
Type
protein-coding
Description
ring finger protein 146
Entrez Gene ID
81847
Genome
hg19
Position
chr6:127,588,009-127,609,707
Genome
hg38
Position
chr6:127,266,864-127,288,562
MIM
612137 OMIM
HGNC
HGNC:21336 HGNC
Ensembl
ENSG00000118518 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
34
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 612137 OMIM
HGNC HGNC:21336 HGNC
Ensembl ENSG00000118518 Ensembl
AllianceGenome HGNC:21336
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000608991.5 hg38 chr6 127,266,883 127,288,362 21,480
ENST00000610153.1 hg38 chr6 127,266,883 127,288,362 21,480
ENST00000368314.6 hg38 chr6 127,266,864 127,288,562 21,699
ENST00000356799.6 hg38 chr6 127,266,849 127,288,567 21,719
ENST00000356799.6 hg19 chr6 127,587,994 127,609,712 21,719
ENST00000368314.6 hg19 chr6 127,588,009 127,609,707 21,699
ENST00000608991.5 hg19 chr6 127,588,028 127,609,507 21,480
ENST00000610153.1 hg19 chr6 127,588,028 127,609,507 21,480
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