SOST sclerostin

Information
Symbol
SOST
Type
protein-coding
Description
sclerostin
Entrez Gene ID
50964
Genome
hg19
Position
chr17:41,831,106-41,836,159
Genome
hg38
Position
chr17:43,753,738-43,758,791
MIM
605740 OMIM
HGNC
HGNC:13771 HGNC
Ensembl
ENSG00000167941 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 10
Likely pathogenic 0 4
Benign 0 22
Likely benign 0 30
Conflicting classifications of pathogenicity 0 8
no classification for the single variant 0 2
not provided 0 16
Uncertain significance 0 80
Ranking
ClinVar
0
0
12
126
6
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 CDD
SYNONYM DAND6
SYNONYM SOST1
SYNONYM VBCH
MIM 605740 OMIM
HGNC HGNC:13771 HGNC
Ensembl ENSG00000167941 Ensembl
AllianceGenome HGNC:13771
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000301691.3 hg38 chr17 43,753,738 43,758,791 5,054
ENST00000301691.3 hg19 chr17 41,831,106 41,836,159 5,054
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