SELENOV selenoprotein V

Information
Symbol
SELENOV
Type
protein-coding
Description
selenoprotein V
Entrez Gene ID
348303
Genome
hg19
Position
chr19:40,005,779-40,011,315
Genome
hg38
Position
chr19:39,515,139-39,520,675
MIM
607919 OMIM
HGNC
HGNC:30399 HGNC
Ensembl
ENSG00000186838 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 60
Ranking
ClinVar
0
0
0
62
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 SELV
MIM 607919 OMIM
HGNC HGNC:30399 HGNC
Ensembl ENSG00000186838 Ensembl
AllianceGenome HGNC:30399
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000335426.9 hg38 chr19 39,515,139 39,520,675 5,537
ENST00000335426.9 hg19 chr19 40,005,779 40,011,315 5,537
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