SLC17A9 solute carrier family 17 member 9

Information
Symbol
SLC17A9
Type
protein-coding
Description
solute carrier family 17 member 9
Entrez Gene ID
63910
Genome
hg19
Position
chr20:61,584,061-61,600,937
Genome
hg38
Position
chr20:62,952,709-62,969,585
MIM
612107 OMIM
HGNC
HGNC:16192 HGNC
Ensembl
ENSG00000101194 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 20
Likely benign 0 30
Uncertain significance 0 50
Ranking
ClinVar
0
0
8
90
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 :
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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 C20orf59
SYNONYM POROK8
SYNONYM VNUT
MIM 612107 OMIM
HGNC HGNC:16192 HGNC
Ensembl ENSG00000101194 Ensembl
AllianceGenome HGNC:16192
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000370349.7 hg38 chr20 62,952,707 62,968,597 15,891
ENST00000370351.9 hg38 chr20 62,952,709 62,969,585 16,877
ENST00000370349.7 hg19 chr20 61,584,059 61,599,949 15,891
ENST00000370351.9 hg19 chr20 61,584,061 61,600,937 16,877
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