Product Details

SNP ID

rs201705374

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:7089131 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTCGACCGGCAAACATGGTTGAAG[C/G]GGATCGCCCGGGGAAGCTGTTCATT

Phenotype

MIM: 609665 MIM: 605444

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

NLRP14 PubMed Links

Additional Information

For this assay, SNP(s) [rs4758158] 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

NLRP14

Gene Name

NLR family pyrin domain containing 14

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_176822.3	198	Intron			NP_789792.1
XM_011520044.1	198	Intron			XP_011518346.1

Gene

RBMXL2

Gene Name

RNA binding motif protein, X-linked like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014469.4	198	Missense Mutation	GCG,GGG	A4G	NP_055284.3

View Full Product Details