TRIM49B tripartite motif containing 49B

Information
Symbol
TRIM49B
Type
protein-coding
Description
tripartite motif containing 49B
Entrez Gene ID
283116
Genome
hg19
Position
chr11:49,049,053-49,060,003
Genome
hg38
Position
chr11:49,027,501-49,038,451
HGNC
HGNC:42955 HGNC
Ensembl
ENSG00000182053 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 10
Uncertain significance 0 64
Ranking
ClinVar
0
0
0
76
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:42955 HGNC
Ensembl ENSG00000182053 Ensembl
AllianceGenome HGNC:42955
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000332682.9 hg38 chr11 49,028,823 49,038,155 9,333
ENST00000622138.4 hg38 chr11 49,027,501 49,038,451 10,951
ENST00000622138.4 hg19 chr11 49,049,053 49,060,003 10,951
ENST00000332682.9 hg19 chr11 49,050,375 49,059,707 9,333
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