SLC38A3 solute carrier family 38 member 3

Information
Symbol
SLC38A3
Type
protein-coding
Description
solute carrier family 38 member 3
Entrez Gene ID
10991
Genome
hg19
Position
chr3:50,242,704-50,258,918
Genome
hg38
Position
chr3:50,205,271-50,221,486
MIM
604437 OMIM
HGNC
HGNC:18044 HGNC
Ensembl
ENSG00000188338 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 10
Likely benign 0 4
Uncertain significance 0 54
Ranking
ClinVar
0
0
0
54
14
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 DEE102
SYNONYM G17
SYNONYM NAT1
SYNONYM SN1
SYNONYM SNAT3
MIM 604437 OMIM
HGNC HGNC:18044 HGNC
Ensembl ENSG00000188338 Ensembl
AllianceGenome HGNC:18044
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000614032.5 hg38 chr3 50,205,271 50,221,486 16,216
ENST00000614032.5 hg19 chr3 50,242,704 50,258,918 16,215
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