TRIM43B tripartite motif containing 43B

Information
Symbol
TRIM43B
Type
protein-coding
Description
tripartite motif containing 43B
Entrez Gene ID
653192
Genome
hg19
Position
chr2:96,142,756-96,150,502
Genome
hg38
Position
chr2:95,477,008-95,484,754
HGNC
HGNC:37146 HGNC
Ensembl
ENSG00000144010 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 10
Ranking
ClinVar
0
0
0
12
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
HGNC HGNC:37146 HGNC
Ensembl ENSG00000144010 Ensembl
AllianceGenome HGNC:37146
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000639673.3 hg38 chr2 95,477,008 95,484,754 7,747
ENST00000639673.3 hg19 chr2 96,142,756 96,150,502 7,747
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