Product Details

SNP ID

rs2268996

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.6:87476059 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

GAGCAGGTCTGGGAATAAGGAAGTA[C/T]GAGGGAGACTTGGTACCCACTGCTT

Phenotype

MIM: 605634

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC35A1 PubMed Links

Additional Information

For this assay, SNP(s) [rs10711430] 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

SLC35A1

Gene Name

solute carrier family 35 member A1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001168398.1		Intron			NP_001161870.1
NM_006416.4		Intron			NP_006407.1

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