TRIM39-RPP21 TRIM39-RPP21 readthrough

Information
Symbol
TRIM39-RPP21
Type
protein-coding
Description
TRIM39-RPP21 readthrough
Entrez Gene ID
202658
Genome
hg19
Position
chr6:30,296,684-30,314,631
Genome
hg38
Position
chr6:30,328,907-30,346,854
HGNC
HGNC:38845 HGNC
Ensembl
ENSG00000248167 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
not provided 4 0
Uncertain significance 0 12
Ranking
ClinVar
0
0
0
20
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 TRIM39R
HGNC HGNC:38845 HGNC
Ensembl ENSG00000248167 Ensembl
AllianceGenome HGNC:38845
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000623385.3 hg38 chr6 30,328,907 30,346,854 17,948
ENST00000623385.3 hg19 chr6 30,296,684 30,314,631 17,948
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