Product Details

SNP ID

rs586001

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:30607321 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATAAGGTGAGTAAAACAATGCCTCC[A/G]TTCAATACCCAGCGTTTCTTTTGGG

Phenotype

MIM: 612748

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

LYZL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs533890696] 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

LYZL2

Gene Name

lysozyme like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_183058.2		Intron			NP_898881.2
XM_011519306.2		Intron			XP_011517608.1
XM_011519307.2		Intron			XP_011517609.1

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