TRIM48 tripartite motif containing 48

Information
Symbol
TRIM48
Type
protein-coding
Description
tripartite motif containing 48
Entrez Gene ID
79097
Genome
hg19
Position
chr11:55,029,631-55,038,590
Genome
hg38
Position
chr11:55,262,155-55,271,114
HGNC
HGNC:19021 HGNC
Ensembl
ENSG00000150244 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 50
Ranking
ClinVar
0
0
0
52
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 RNF101
HGNC HGNC:19021 HGNC
Ensembl ENSG00000150244 Ensembl
AllianceGenome HGNC:19021
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000417545.5 hg38 chr11 55,262,155 55,271,114 8,960
ENST00000417545.5 hg19 chr11 55,029,631 55,038,590 8,960
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