Product Details

SNP ID

rs182799009

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:159713585 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTGCACTTCATACTTCAGTGCCCG[C/T]CAGTTCAGGACATTAGGACTGAAGG

Phenotype

MIM: 123260

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CRP PubMed Links

Gene Details

Gene

CRP

Gene Name

C-reactive protein, pentraxin-related

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000567.2	719	Nonsense Mutation	TGA,TGG	*205W	NP_000558.2
XM_011509207.2	719	Nonsense Mutation	TGA,TGG	*205W	XP_011507509.1

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