Product Details

SNP ID

rs141583738

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:159588172 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCATGTAAACTTGATCACACCGCTG[C/G]AGAAGCCTCTACAGAACTTTACCTT

Phenotype

MIM: 104770

Polymorphism

C/G, Transversion 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	232	Missense Mutation	CAG,GAG	Q46E	NP_001630.1

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