SLC17A6 solute carrier family 17 member 6

Information
Symbol
SLC17A6
Type
protein-coding
Description
solute carrier family 17 member 6
Entrez Gene ID
57084
Genome
hg19
Position
chr11:22,359,927-22,401,049
Genome
hg38
Position
chr11:22,338,381-22,379,503
MIM
607563 OMIM
HGNC
HGNC:16703 HGNC
Ensembl
ENSG00000091664 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Uncertain significance 0 52
Ranking
ClinVar
0
0
0
58
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 :
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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 :
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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 DNPI
SYNONYM VGLUT2
MIM 607563 OMIM
HGNC HGNC:16703 HGNC
Ensembl ENSG00000091664 Ensembl
AllianceGenome HGNC:16703
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000263160.4 hg38 chr11 22,338,381 22,379,503 41,123
ENST00000263160.4 hg19 chr11 22,359,927 22,401,049 41,123
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