Product Details

SNP ID

rs659497

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:42537437 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGAATGTGTGCACGCAAAGCTACTC[C/T]TTCGTGTGGTGGGACTGGGCCCGCT

Phenotype

MIM: 609701

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NAGLU PubMed Links

Additional Information

For this assay, SNP(s) [rs61737294] 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

NAGLU

Gene Name

N-acetyl-alpha-glucosaminidase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000263.3	500	Silent Mutation	TCC,TCT	S141S	NP_000254.2
XM_006721920.2	500	UTR 5			XP_006721983.1
XM_011524840.1	500	UTR 5			XP_011523142.1
XM_017024686.1	500	Intron			XP_016880175.1
XM_017024687.1	500	UTR 5			XP_016880176.1

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