Product Details

SNP ID

rs139646181

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:55948094 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCAAGCAGCTCTTACTGACTGAGCT[C/T]AGTACTGGCACCATGCCCATCACCT

Phenotype

MIM: 609659

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NLRP8 PubMed Links

Additional Information

For this assay, SNP(s) [rs61195059] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

NLRP8

Gene Name

NLR family pyrin domain containing 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317000.1	263	Silent Mutation	CTC,CTT	L64L	NP_001303929.1
NM_176811.2	263	Silent Mutation	CTC,CTT	L64L	NP_789781.2

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