Product Details

SNP ID

rs13826

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:34562906 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGTATGACGAGTGCACGATGATGGA[C/T]CACTGTCATGGGGAACACAGTGCGG

Phenotype

MIM: 606098

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SNX6 PubMed Links

Additional Information

For this assay, SNP(s) [rs113133395] 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

SNX6

Gene Name

sorting nexin 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021249.3	1586	UTR 3			NP_067072.3
NM_152233.2	1586	UTR 3			NP_689419.2
XM_006720224.1	1586	UTR 3			XP_006720287.1

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