SLC38A10 solute carrier family 38 member 10

Information
Symbol
SLC38A10
Type
protein-coding
Description
solute carrier family 38 member 10
Entrez Gene ID
124565
Genome
hg19
Position
chr17:79,218,611-79,269,107
Genome
hg38
Position
chr17:81,244,811-81,295,307
MIM
616525 OMIM
HGNC
HGNC:28237 HGNC
Ensembl
ENSG00000157637 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 24
Uncertain significance 0 110
Ranking
ClinVar
0
0
0
136
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
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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 :
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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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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 PP1744
SYNONYM SNAT10
MIM 616525 OMIM
HGNC HGNC:28237 HGNC
Ensembl ENSG00000157637 Ensembl
AllianceGenome HGNC:28237
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000288439.9 hg38 chr17 81,251,196 81,295,267 44,072
ENST00000374759.8 hg38 chr17 81,244,811 81,295,307 50,497
ENST00000374759.8 hg19 chr17 79,218,611 79,269,107 50,497
ENST00000288439.9 hg19 chr17 79,224,996 79,269,067 44,072
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