STX10 syntaxin 10

Information
Symbol
STX10
Type
protein-coding
Description
syntaxin 10
Entrez Gene ID
8677
Genome
hg19
Position
chr19:13,254,872-13,261,189
Genome
hg38
Position
chr19:13,144,058-13,150,375
MIM
603765 OMIM
HGNC
HGNC:11428 HGNC
Ensembl
ENSG00000104915 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
32
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 SYN10
SYNONYM hsyn10
MIM 603765 OMIM
HGNC HGNC:11428 HGNC
Ensembl ENSG00000104915 Ensembl
AllianceGenome HGNC:11428
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000343587.9 hg38 chr19 13,144,058 13,150,346 6,289
ENST00000242770.9 hg38 chr19 13,144,062 13,150,178 6,117
ENST00000589083.5 hg38 chr19 13,144,062 13,150,226 6,165
ENST00000587230.6 hg38 chr19 13,144,058 13,150,375 6,318
ENST00000343587.9 hg19 chr19 13,254,872 13,261,160 6,289
ENST00000587230.6 hg19 chr19 13,254,872 13,261,189 6,318
ENST00000242770.9 hg19 chr19 13,254,876 13,260,992 6,117
ENST00000589083.5 hg19 chr19 13,254,876 13,261,040 6,165
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