APCS amyloid P component, serum

Information
Symbol
APCS
Type
protein-coding
Description
amyloid P component, serum
Entrez Gene ID
325
Genome
hg19
Position
chr1:159,557,616-159,558,655
Genome
hg38
Position
chr1:159,587,826-159,588,865
MIM
104770 OMIM
HGNC
HGNC:584 HGNC
Ensembl
ENSG00000132703 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
24
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
SYNONYM HEL-S-92n
SYNONYM PTX2
SYNONYM SAP
MIM 104770 OMIM
HGNC HGNC:584 HGNC
Ensembl ENSG00000132703 Ensembl
AllianceGenome HGNC:584
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000255040.3 hg38 chr1 159,587,826 159,588,865 1,040
ENST00000255040.3 hg19 chr1 159,557,616 159,558,655 1,040
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