S100A13 S100 calcium binding protein A13

Information
Symbol
S100A13
Type
protein-coding
Description
S100 calcium binding protein A13
Entrez Gene ID
6284
Genome
hg19
Position
chr1:153,591,263-153,600,724
Genome
hg38
Position
chr1:153,618,787-153,628,248
MIM
601989 OMIM
HGNC
HGNC:10490 HGNC
Ensembl
ENSG00000189171 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
16
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 :
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
MIM 601989 OMIM
HGNC HGNC:10490 HGNC
Ensembl ENSG00000189171 Ensembl
AllianceGenome HGNC:10490
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000476133.6 hg38 chr1 153,618,799 153,627,505 8,707
ENST00000339556.8 hg38 chr1 153,618,799 153,628,180 9,382
ENST00000440685.7 hg38 chr1 153,618,787 153,628,248 9,462
ENST00000392623.5 hg38 chr1 153,618,804 153,627,268 8,465
ENST00000392622.3 hg38 chr1 153,618,804 153,627,048 8,245
ENST00000440685.7 hg19 chr1 153,591,263 153,600,724 9,462
ENST00000476133.6 hg19 chr1 153,591,275 153,599,981 8,707
ENST00000339556.8 hg19 chr1 153,591,275 153,600,656 9,382
ENST00000392622.3 hg19 chr1 153,591,280 153,599,524 8,245
ENST00000392623.5 hg19 chr1 153,591,280 153,599,744 8,465
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