Product Details

SNP ID

rs35176975

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:27549367 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGTATTAAGAATTTACAATCAACC[A/G]CCTCCTCTCTGCTGGTGATGATGTC

Phenotype

MIM: 609733

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

LNX2 PubMed Links

Additional Information

For this assay, SNP(s) [rs141847682] 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

LNX2

Gene Name

ligand of numb-protein X 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_153371.3		Intron			NP_699202.1
XM_011534995.2		Intron			XP_011533297.1
XM_017020434.1		Intron			XP_016875923.1

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