Product Details

SNP ID

rs10766390

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:17365402 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGTTGATGTGGTAGTAAAGTGTTG[G/T]AGGAGAATCTGTTTATACTTTTATG

Phenotype

MIM: 613714

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

NCR3LG1 PubMed Links

Additional Information

For this assay, SNP(s) [rs72865031] 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

NCR3LG1

Gene Name

natural killer cell cytotoxicity receptor 3 ligand 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001202439.2		Intron			NP_001189368.1
XM_011520072.2		Intron			XP_011518374.1
XM_011520073.2		Intron			XP_011518375.1
XM_011520074.2		Intron			XP_011518376.1
XM_011520075.2		Intron			XP_011518377.1

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