SLC25A10 solute carrier family 25 member 10

Information
Symbol
SLC25A10
Type
protein-coding
Description
solute carrier family 25 member 10
Entrez Gene ID
1468
Genome
hg19
Position
chr17:79,679,266-79,688,046
Genome
hg38
Position
chr17:81,712,236-81,721,016
MIM
606794 OMIM
HGNC
HGNC:10980 HGNC
Ensembl
ENSG00000183048 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 4
Benign 0 12
Likely benign 0 22
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 40
Ranking
ClinVar
0
0
10
64
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 :
Search word :
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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 DIC
SYNONYM MTDPS19
MIM 606794 OMIM
HGNC HGNC:10980 HGNC
Ensembl ENSG00000183048 Ensembl
AllianceGenome HGNC:10980
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000350690.10 hg38 chr17 81,712,284 81,721,012 8,729
ENST00000545862.5 hg38 chr17 81,712,236 81,721,016 8,781
ENST00000331531.9 hg38 chr17 81,712,307 81,721,012 8,706
ENST00000545862.5 hg19 chr17 79,679,266 79,688,046 8,781
ENST00000350690.10 hg19 chr17 79,679,314 79,688,042 8,729
ENST00000331531.9 hg19 chr17 79,679,337 79,688,042 8,706
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