SLC25A20 solute carrier family 25 member 20

Information
Symbol
SLC25A20
Type
protein-coding
Description
solute carrier family 25 member 20
Entrez Gene ID
788
Genome
hg19
Position
chr3:48,894,359-48,936,315
Genome
hg38
Position
chr3:48,856,926-48,898,882
MIM
613698 OMIM
HGNC
HGNC:1421 HGNC
Ensembl
ENSG00000178537 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 8 88
Likely pathogenic 0 46
Benign 0 16
Likely benign 0 238
Conflicting classifications of pathogenicity 0 20
Uncertain significance 0 186
Ranking
ClinVar
0
0
98
452
6
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
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 CAC
SYNONYM CACT
MIM 613698 OMIM
HGNC HGNC:1421 HGNC
Ensembl ENSG00000178537 Ensembl
AllianceGenome HGNC:1421
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000430379.5 hg38 chr3 48,856,931 48,898,904 41,974
ENST00000319017.5 hg38 chr3 48,856,926 48,898,882 41,957
ENST00000319017.5 hg19 chr3 48,894,359 48,936,315 41,957
ENST00000430379.5 hg19 chr3 48,894,364 48,936,337 41,974
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