SNX22 sorting nexin 22

Information
Symbol
SNX22
Type
protein-coding
Description
sorting nexin 22
Entrez Gene ID
79856
Genome
hg19
Position
chr15:64,443,930-64,449,680
Genome
hg38
Position
chr15:64,151,731-64,157,481
HGNC
HGNC:16315 HGNC
Ensembl
ENSG00000157734 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 8
Benign 0 12
Likely benign 0 30
Conflicting classifications of pathogenicity 0 8
not provided 0 4
Uncertain significance 0 72
Ranking
ClinVar
0
0
20
100
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
[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
HGNC HGNC:16315 HGNC
Ensembl ENSG00000157734 Ensembl
AllianceGenome HGNC:16315
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000325881.9 hg38 chr15 64,151,731 64,157,481 5,751
ENST00000325881.9 hg19 chr15 64,443,930 64,449,680 5,751
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