CAPS2 calcyphosine 2

Information
Symbol
CAPS2
Type
protein-coding
Description
calcyphosine 2
Entrez Gene ID
84698
Genome
hg19
Position
chr12:75,669,759-75,724,104
Genome
hg38
Position
chr12:75,275,979-75,330,324
MIM
607724 OMIM
HGNC
HGNC:16471 HGNC
Ensembl
ENSG00000180881 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 6
Uncertain significance 0 74
Ranking
ClinVar
0
0
0
86
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 UG0636c06
MIM 607724 OMIM
HGNC HGNC:16471 HGNC
Ensembl ENSG00000180881 Ensembl
AllianceGenome HGNC:16471
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409445.8 hg38 chr12 75,275,979 75,330,056 54,078
ENST00000393284.8 hg38 chr12 75,277,211 75,326,498 49,288
ENST00000699294.1 hg38 chr12 75,275,979 75,330,324 54,346
ENST00000409799.6 hg38 chr12 75,275,979 75,330,025 54,047
ENST00000409799.6 hg19 chr12 75,669,759 75,723,805 54,047
ENST00000409445.8 hg19 chr12 75,669,759 75,723,836 54,078
ENST00000699294.1 hg19 chr12 75,669,759 75,724,104 54,346
ENST00000393284.8 hg19 chr12 75,670,991 75,720,278 49,288
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