SNAP29 synaptosome associated protein 29

Information
Symbol
SNAP29
Type
protein-coding
Description
synaptosome associated protein 29
Entrez Gene ID
9342
Genome
hg19
Position
chr22:21,213,295-21,245,502
Genome
hg38
Position
chr22:20,859,007-20,891,214
MIM
604202 OMIM
HGNC
HGNC:11133 HGNC
Ensembl
ENSG00000099940 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 28
Likely pathogenic 0 12
Benign 0 82
Likely benign 0 234
Conflicting classifications of pathogenicity 0 18
not provided 14 0
Uncertain significance 0 280
Ranking
ClinVar
0
0
62
554
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 CEDNIK
SYNONYM SNAP-29
MIM 604202 OMIM
HGNC HGNC:11133 HGNC
Ensembl ENSG00000099940 Ensembl
AllianceGenome HGNC:11133
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000215730.12 hg38 chr22 20,859,007 20,891,214 32,208
ENST00000215730.12 hg19 chr22 21,213,295 21,245,502 32,208
Genome browser