Product Details

SNP ID

rs12684502

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:88539458 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTTGGGGAAGAGGTTCCAGGTTCCT[A/G]AGATAACAGAGTCCCACCTGGTCTG

Phenotype

MIM: 615299

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

NXNL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs114905411] 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

NXNL2

Gene Name

nucleoredoxin-like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001161625.1		Intron			NP_001155097.1
NM_145283.2		Intron			NP_660326.2
XM_005251727.3		Intron			XP_005251784.1
XM_011518275.2		Intron			XP_011516577.1
XM_011518276.2		Intron			XP_011516578.1

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