Product Details

SNP ID

rs11545897

Assay Type

Functionally tested

NCBI dbSNP Submissions

29

Location

Chr.1:159587931 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCCTAGGCCAGGAATATGAACAAG[C/T]CGCTGCTTTGGATCTCTGTCCTCAC

Phenotype

MIM: 104770

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

APCS PubMed Links

Gene Details

Gene

APCS

Gene Name

amyloid P component, serum

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001639.3	106	Missense Mutation	CCG,TCG	P4S	NP_001630.1

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