SNX33 sorting nexin 33

Information
Symbol
SNX33
Type
protein-coding
Description
sorting nexin 33
Entrez Gene ID
257364
Genome
hg19
Position
chr15:75,940,253-75,954,642
Genome
hg38
Position
chr15:75,647,912-75,662,301
MIM
619107 OMIM
HGNC
HGNC:28468 HGNC
Ensembl
ENSG00000173548 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
not provided 1 0
Uncertain significance 0 56
Ranking
ClinVar
0
0
0
60
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
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 SH3PX3
SYNONYM SH3PXD3C
SYNONYM SNX30
MIM 619107 OMIM
HGNC HGNC:28468 HGNC
Ensembl ENSG00000173548 Ensembl
AllianceGenome HGNC:28468
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000308527.6 hg38 chr15 75,647,912 75,662,301 14,390
ENST00000308527.6 hg19 chr15 75,940,253 75,954,642 14,390
Genome browser