SLC7A10 solute carrier family 7 member 10

Information
Symbol
SLC7A10
Type
protein-coding
Description
solute carrier family 7 member 10
Entrez Gene ID
56301
Genome
hg19
Position
chr19:33,699,570-33,716,756
Genome
hg38
Position
chr19:33,208,664-33,225,850
MIM
607959 OMIM
HGNC
HGNC:11058 HGNC
Ensembl
ENSG00000130876 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 28
Likely benign 0 20
Uncertain significance 0 64
Ranking
ClinVar
0
0
0
112
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 ASC1
SYNONYM HASC-1
SYNONYM asc-1
MIM 607959 OMIM
HGNC HGNC:11058 HGNC
Ensembl ENSG00000130876 Ensembl
AllianceGenome HGNC:11058
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000253188.8 hg38 chr19 33,208,664 33,225,850 17,187
ENST00000253188.8 hg19 chr19 33,699,570 33,716,756 17,187
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