SNX19 sorting nexin 19

Information
Symbol
SNX19
Type
protein-coding
Description
sorting nexin 19
Entrez Gene ID
399979
Genome
hg19
Position
chr11:130,736,145-130,786,374
Genome
hg38
Position
chr11:130,866,250-130,916,479
HGNC
HGNC:21532 HGNC
Ensembl
ENSG00000120451 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 18
not provided 0 2
Uncertain significance 0 120
Ranking
ClinVar
0
0
2
142
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 CHET8
HGNC HGNC:21532 HGNC
Ensembl ENSG00000120451 Ensembl
AllianceGenome HGNC:21532
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000533214.1 hg38 chr11 130,905,655 130,916,449 10,795
ENST00000530356.5 hg38 chr11 130,878,393 130,916,451 38,059
ENST00000426933.6 hg38 chr11 130,878,051 130,893,874 15,824
ENST00000528555.5 hg38 chr11 130,878,393 130,916,451 38,059
ENST00000534726.5 hg38 chr11 130,877,958 130,908,346 30,389
ENST00000265909.9 hg38 chr11 130,866,250 130,916,479 50,230
ENST00000265909.9 hg19 chr11 130,736,145 130,786,374 50,230
ENST00000534726.5 hg19 chr11 130,747,853 130,778,241 30,389
ENST00000426933.6 hg19 chr11 130,747,946 130,763,769 15,824
ENST00000528555.5 hg19 chr11 130,748,288 130,786,346 38,059
ENST00000530356.5 hg19 chr11 130,748,288 130,786,346 38,059
ENST00000533214.1 hg19 chr11 130,775,550 130,786,344 10,795
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