SLC17A7 solute carrier family 17 member 7

Information
Symbol
SLC17A7
Type
protein-coding
Description
solute carrier family 17 member 7
Entrez Gene ID
57030
Genome
hg19
Position
chr19:49,932,658-49,944,784
Genome
hg38
Position
chr19:49,429,401-49,441,527
MIM
605208 OMIM
HGNC
HGNC:16704 HGNC
Ensembl
ENSG00000104888 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 12
Likely benign 0 4
Uncertain significance 0 32
Ranking
ClinVar
0
0
0
48
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 :
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 BNPI
SYNONYM VGLUT1
MIM 605208 OMIM
HGNC HGNC:16704 HGNC
Ensembl ENSG00000104888 Ensembl
AllianceGenome HGNC:16704
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000600601.5 hg38 chr19 49,429,986 49,442,360 12,375
ENST00000221485.8 hg38 chr19 49,429,401 49,441,527 12,127
ENST00000221485.8 hg19 chr19 49,932,658 49,944,784 12,127
ENST00000600601.5 hg19 chr19 49,933,243 49,945,617 12,375
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