TRIM56 tripartite motif containing 56

Information
Symbol
TRIM56
Type
protein-coding
Description
tripartite motif containing 56
Entrez Gene ID
81844
Genome
hg19
Position
chr7:100,728,762-100,741,248
Genome
hg38
Position
chr7:101,085,481-101,097,967
MIM
616996 OMIM
HGNC
HGNC:19028 HGNC
Ensembl
ENSG00000169871 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 10
Uncertain significance 0 102
Ranking
ClinVar
0
0
0
116
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 RNF109
MIM 616996 OMIM
HGNC HGNC:19028 HGNC
Ensembl ENSG00000169871 Ensembl
AllianceGenome HGNC:19028
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000306085.11 hg38 chr7 101,085,481 101,097,967 12,487
ENST00000306085.11 hg19 chr7 100,728,762 100,741,248 12,487
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