TRIM38 tripartite motif containing 38

Information
Symbol
TRIM38
Type
protein-coding
Description
tripartite motif containing 38
Entrez Gene ID
10475
Genome
hg19
Position
chr6:25,963,030-25,991,459
Genome
hg38
Position
chr6:25,962,802-25,991,231
HGNC
HGNC:10059 HGNC
Ensembl
ENSG00000112343 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 16 0
Uncertain significance 0 48
Ranking
ClinVar
0
0
0
48
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 RNF15
SYNONYM RORET
HGNC HGNC:10059 HGNC
Ensembl ENSG00000112343 Ensembl
AllianceGenome HGNC:10059
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000357085.5 hg38 chr6 25,962,802 25,991,231 28,430
ENST00000357085.5 hg19 chr6 25,963,030 25,991,459 28,430
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