SELENOT selenoprotein T

Information
Symbol
SELENOT
Type
protein-coding
Description
selenoprotein T
Entrez Gene ID
51714
Genome
hg19
Position
chr3:150,321,108-150,348,223
Genome
hg38
Position
chr3:150,603,321-150,630,436
MIM
607912 OMIM
HGNC
HGNC:18136 HGNC
Ensembl
ENSG00000198843 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 12
Ranking
ClinVar
0
0
0
12
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 :
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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 SELT
MIM 607912 OMIM
HGNC HGNC:18136 HGNC
Ensembl ENSG00000198843 Ensembl
AllianceGenome HGNC:18136
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000477889.5 hg38 chr3 150,603,291 150,627,693 24,403
ENST00000471696.6 hg38 chr3 150,603,321 150,630,436 27,116
ENST00000485923.1 hg38 chr3 150,603,336 150,627,905 24,570
ENST00000480740.5 hg38 chr3 150,602,875 150,627,831 24,957
ENST00000480740.5 hg19 chr3 150,320,662 150,345,618 24,957
ENST00000477889.5 hg19 chr3 150,321,078 150,345,480 24,403
ENST00000471696.6 hg19 chr3 150,321,108 150,348,223 27,116
ENST00000485923.1 hg19 chr3 150,321,123 150,345,692 24,570
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