TSEN34 tRNA splicing endonuclease subunit 34

Information
Symbol
TSEN34
Type
protein-coding
Description
tRNA splicing endonuclease subunit 34
Entrez Gene ID
79042
Genome
hg19
Position
chr19:54,694,138-54,697,585
Genome
hg38
Position
chr19:54,190,287-54,193,730
MIM
608754 OMIM
HGNC
HGNC:15506 HGNC
Ensembl
ENSG00000170892 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Likely pathogenic 0 2
Benign 0 60
Likely benign 0 91
Conflicting classifications of pathogenicity 0 16
Uncertain significance 0 156
Ranking
ClinVar
0
0
55
242
4
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 LENG5
SYNONYM PCH2C
SYNONYM SEN34
SYNONYM SEN34L
MIM 608754 OMIM
HGNC HGNC:15506 HGNC
Ensembl ENSG00000170892 Ensembl
AllianceGenome HGNC:15506
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000429671.7 hg38 chr19 54,190,268 54,194,532 4,265
ENST00000653273.2 hg38 chr19 54,191,306 54,194,532 3,227
ENST00000665674.2 hg38 chr19 54,190,738 54,194,532 3,795
ENST00000667261.1 hg38 chr19 54,190,287 54,193,730 3,444
ENST00000302937.8 hg38 chr19 54,190,268 54,194,536 4,269
ENST00000396388.3 hg38 chr19 54,191,308 54,194,532 3,225
ENST00000396383.5 hg38 chr19 54,190,731 54,193,666 2,936
ENST00000455798.6 hg38 chr19 54,189,938 54,194,532 4,595
ENST00000455798.6 hg19 chr19 54,693,789 54,698,390 4,602
ENST00000429671.7 hg19 chr19 54,694,119 54,698,390 4,272
ENST00000302937.8 hg19 chr19 54,694,119 54,698,394 4,276
ENST00000667261.1 hg19 chr19 54,694,138 54,697,585 3,448
ENST00000396383.5 hg19 chr19 54,694,582 54,697,521 2,940
ENST00000665674.2 hg19 chr19 54,694,589 54,698,390 3,802
ENST00000653273.2 hg19 chr19 54,695,157 54,698,390 3,234
ENST00000396388.3 hg19 chr19 54,695,159 54,698,390 3,232
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