SNX32 sorting nexin 32

Information
Symbol
SNX32
Type
protein-coding
Description
sorting nexin 32
Entrez Gene ID
254122
Genome
hg19
Position
chr11:65,601,434-65,621,172
Genome
hg38
Position
chr11:65,833,963-65,853,701
HGNC
HGNC:26423 HGNC
Ensembl
ENSG00000172803 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 80
Ranking
ClinVar
0
0
0
82
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 SNX6B
HGNC HGNC:26423 HGNC
Ensembl ENSG00000172803 Ensembl
AllianceGenome HGNC:26423
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000308342.7 hg38 chr11 65,833,963 65,853,701 19,739
ENST00000308342.7 hg19 chr11 65,601,434 65,621,172 19,739
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