Product Details

SNP ID

rs289736

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:56997298 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAATGGGGAGGTGCAGGTGGAATAC[C/T]GTAGCCTGATGCCCAGCCTATGCCG

Phenotype

MIM: 613537

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NLRC5 PubMed Links

Additional Information

For this assay, SNP(s) [rs76174399] are located under a primer 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

NLRC5

Gene Name

NLR family CARD domain containing 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032206.4		Intron			NP_115582.4
XM_005256193.2		Intron			XP_005256250.1
XM_005256194.3		Intron			XP_005256251.1
XM_005256195.2		Intron			XP_005256252.1
XM_005256196.2		Intron			XP_005256253.1
XM_005256197.2		Intron			XP_005256254.1
XM_005256199.3		Intron			XP_005256256.1
XM_005256201.3		Intron			XP_005256258.1
XM_006721297.2		Intron			XP_006721360.1
XM_006721298.2		Intron			XP_006721361.1
XM_006721300.2		Intron			XP_006721363.1
XM_011523373.2		Intron			XP_011521675.1
XM_011523375.2		Intron			XP_011521677.1
XM_011523376.2		Intron			XP_011521678.1
XM_017023766.1		Intron			XP_016879255.1
XM_017023767.1		Intron			XP_016879256.1
XM_017023768.1		Intron			XP_016879257.1
XM_017023769.1		Intron			XP_016879258.1
XM_017023770.1		Intron			XP_016879259.1
XM_017023771.1		Intron			XP_016879260.1

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