S100A14 S100 calcium binding protein A14

Information
Symbol
S100A14
Type
protein-coding
Description
S100 calcium binding protein A14
Entrez Gene ID
57402
Genome
hg19
Position
chr1:153,586,731-153,589,462
Genome
hg38
Position
chr1:153,614,255-153,616,986
MIM
607986 OMIM
HGNC
HGNC:18901 HGNC
Ensembl
ENSG00000189334 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 12
Ranking
ClinVar
0
0
0
12
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 :
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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 BCMP84
SYNONYM S100A15
MIM 607986 OMIM
HGNC HGNC:18901 HGNC
Ensembl ENSG00000189334 Ensembl
AllianceGenome HGNC:18901
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000476873.5 hg38 chr1 153,614,255 153,615,938 1,684
ENST00000344616.4 hg38 chr1 153,614,255 153,616,325 2,071
ENST00000368702.5 hg38 chr1 153,614,255 153,616,986 2,732
ENST00000368701.5 hg38 chr1 153,614,255 153,616,289 2,035
ENST00000476873.5 hg19 chr1 153,586,731 153,588,414 1,684
ENST00000368701.5 hg19 chr1 153,586,731 153,588,765 2,035
ENST00000344616.4 hg19 chr1 153,586,731 153,588,801 2,071
ENST00000368702.5 hg19 chr1 153,586,731 153,589,462 2,732
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