Product Details

SNP ID

rs7769948

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:157716982 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAATCCCATGCCCGTCTGTCATCTC[C/T]GCACTTGCTGGGCTGCATTTTACTG

Phenotype

MIM: 605952

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SNX9 PubMed Links

Additional Information

For this assay, SNP(s) [rs111627075] 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

SNX9

Gene Name

sorting nexin 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016224.4		Intron			NP_057308.1
XM_005267015.2		Intron			XP_005267072.1
XM_011535886.2		Intron			XP_011534188.1

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