SNX17 sorting nexin 17

Information
Symbol
SNX17
Type
protein-coding
Description
sorting nexin 17
Entrez Gene ID
9784
Genome
hg19
Position
chr2:27,593,483-27,600,402
Genome
hg38
Position
chr2:27,370,616-27,377,535
MIM
605963 OMIM
HGNC
HGNC:14979 HGNC
Ensembl
ENSG00000115234 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 10
Uncertain significance 0 68
Ranking
ClinVar
0
0
0
78
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
MIM 605963 OMIM
HGNC HGNC:14979 HGNC
Ensembl ENSG00000115234 Ensembl
AllianceGenome HGNC:14979
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000233575.7 hg38 chr2 27,370,616 27,377,535 6,920
ENST00000537606.5 hg38 chr2 27,370,496 27,377,533 7,038
ENST00000537606.5 hg19 chr2 27,593,363 27,600,400 7,038
ENST00000233575.7 hg19 chr2 27,593,483 27,600,402 6,920
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