TRIM49C tripartite motif containing 49C

Information
Symbol
TRIM49C
Type
protein-coding
Description
tripartite motif containing 49C
Entrez Gene ID
642612
Genome
hg19
Position
chr11:89,764,274-89,775,193
Genome
hg38
Position
chr11:90,031,106-90,042,025
HGNC
HGNC:38877 HGNC
Ensembl
ENSG00000204449 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 10
Uncertain significance 0 42
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 TRIM49L2
HGNC HGNC:38877 HGNC
Ensembl ENSG00000204449 Ensembl
AllianceGenome HGNC:38877
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000448984.1 hg38 chr11 90,031,106 90,042,025 10,920
ENST00000448984.1 hg19 chr11 89,764,274 89,775,193 10,920
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