SLC25A35 solute carrier family 25 member 35

Information
Symbol
SLC25A35
Type
protein-coding
Description
solute carrier family 25 member 35
Entrez Gene ID
399512
Genome
hg19
Position
chr17:8,193,379-8,198,718
Genome
hg38
Position
chr17:8,290,061-8,295,400
MIM
610818 OMIM
HGNC
HGNC:31921 HGNC
Ensembl
ENSG00000125434 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 22
Likely benign 0 128
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 192
Ranking
ClinVar
0
0
44
296
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 :
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
MIM 610818 OMIM
HGNC HGNC:31921 HGNC
Ensembl ENSG00000125434 Ensembl
AllianceGenome HGNC:31921
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000577745.2 hg38 chr17 8,290,061 8,295,400 5,340
ENST00000580340.5 hg38 chr17 8,288,861 8,294,838 5,978
ENST00000380067.6 hg38 chr17 8,287,764 8,294,852 7,089
ENST00000579192.5 hg38 chr17 8,287,763 8,295,343 7,581
ENST00000579192.5 hg19 chr17 8,191,081 8,198,661 7,581
ENST00000380067.6 hg19 chr17 8,191,082 8,198,170 7,089
ENST00000580340.5 hg19 chr17 8,192,179 8,198,156 5,978
ENST00000577745.2 hg19 chr17 8,193,379 8,198,718 5,340
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