SELENOF selenoprotein F

Information
Symbol
SELENOF
Type
protein-coding
Description
selenoprotein F
Entrez Gene ID
9403
Genome
hg19
Position
chr1:87,328,128-87,379,809
Genome
hg38
Position
chr1:86,862,445-86,914,126
MIM
606254 OMIM
HGNC
HGNC:17705 HGNC
Ensembl
ENSG00000183291 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 16
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
[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 SEP15
MIM 606254 OMIM
HGNC HGNC:17705 HGNC
Ensembl ENSG00000183291 Ensembl
AllianceGenome HGNC:17705
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000370554.5 hg38 chr1 86,862,725 86,914,134 51,410
ENST00000331835.10 hg38 chr1 86,862,445 86,914,126 51,682
ENST00000401030.4 hg38 chr1 86,863,301 86,914,126 50,826
ENST00000331835.10 hg19 chr1 87,328,128 87,379,809 51,682
ENST00000370554.5 hg19 chr1 87,328,408 87,379,817 51,410
ENST00000401030.4 hg19 chr1 87,328,984 87,379,809 50,826
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