SYCN syncollin

Information
Symbol
SYCN
Type
protein-coding
Description
syncollin
Entrez Gene ID
342898
Genome
hg19
Position
chr19:39,693,465-39,694,903
Genome
hg38
Position
chr19:39,202,825-39,204,263
MIM
620140 OMIM
HGNC
HGNC:18442 HGNC
Ensembl
ENSG00000179751 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 20
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 INSSA1
SYNONYM SYL
MIM 620140 OMIM
HGNC HGNC:18442 HGNC
Ensembl ENSG00000179751 Ensembl
AllianceGenome HGNC:18442
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000318438.7 hg38 chr19 39,202,825 39,204,263 1,439
ENST00000318438.7 hg19 chr19 39,693,465 39,694,903 1,439
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