Product Details

SNP ID

rs201429667

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:99533276 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCACTCTGCGCCCTGCATGCTGGCC[A/G]CCGCTGAGGGGACGCAATTTTCTGA

Phenotype

MIM: 606727

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

LINC01475 PubMed Links

Additional Information

For this assay, SNP(s) [rs41290504] 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

LINC01475

Gene Name

long intergenic non-protein coding RNA 1475

There are no transcripts associated with this gene.

Gene

NKX2-3

Gene Name

NK2 homeobox 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_145285.2	344	Missense Mutation	ACC,GCC	T49A	NP_660328.2
XM_011539370.1	344	Missense Mutation	ACC,GCC	T49A	XP_011537672.1

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