TRIM40 tripartite motif containing 40

Information
Symbol
TRIM40
Type
protein-coding
Description
tripartite motif containing 40
Entrez Gene ID
135644
Genome
hg19
Position
chr6:30,103,917-30,116,505
Genome
hg38
Position
chr6:30,136,140-30,148,728
MIM
616976 OMIM
HGNC
HGNC:18736 HGNC
Ensembl
ENSG00000204614 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 8
not provided 3 0
Uncertain significance 0 20
Ranking
ClinVar
0
0
0
30
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 RNF35
MIM 616976 OMIM
HGNC HGNC:18736 HGNC
Ensembl ENSG00000204614 Ensembl
AllianceGenome HGNC:18736
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000376724.6 hg38 chr6 30,136,731 30,148,735 12,005
ENST00000307859.4 hg38 chr6 30,137,010 30,148,735 11,726
ENST00000396581.6 hg38 chr6 30,136,140 30,148,728 12,589
ENST00000396581.6 hg19 chr6 30,103,917 30,116,505 12,589
ENST00000376724.6 hg19 chr6 30,104,508 30,116,512 12,005
ENST00000307859.4 hg19 chr6 30,104,787 30,116,512 11,726
Genome browser