TRIM49D1 tripartite motif containing 49D1

Information
Symbol
TRIM49D1
Type
protein-coding
Description
tripartite motif containing 49D1
Entrez Gene ID
399939
Genome
hg19
Position
chr11:89,644,279-89,654,935
Genome
hg38
Position
chr11:89,911,111-89,921,767
HGNC
HGNC:43973 HGNC
Ensembl
ENSG00000223417 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
18
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 TRIM49D
SYNONYM TRIM49D1P
SYNONYM TRIM49D2
SYNONYM TRIM49D2P
SYNONYM TRIM49DP
HGNC HGNC:43973 HGNC
Ensembl ENSG00000223417 Ensembl
AllianceGenome HGNC:43973
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000420869.3 hg38 chr11 89,911,409 89,922,245 10,837
ENST00000605881.5 hg38 chr11 89,911,407 89,920,428 9,022
ENST00000530311.6 hg38 chr11 89,911,111 89,921,767 10,657
ENST00000530311.2 hg19 chr11 89,644,279 89,654,935 10,657
ENST00000420869.1 hg19 chr11 89,644,590 89,653,576 8,987
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