Product Details

SNP ID

rs6003929

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:23863346 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTCCTGCTGGTTTGCTCTCAGCAT[C/T]TGAGTCATCTTTGAATCTCTGGCCC

Phenotype

MIM: 610367

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC2A11 PubMed Links

Additional Information

For this assay, SNP(s) [rs372709134] 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

SLC2A11

Gene Name

solute carrier family 2 member 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001024938.3		Intron			NP_001020109.1
NM_001024939.3		Intron			NP_001020110.1
NM_001282864.1		Intron			NP_001269793.1
NM_030807.4		Intron			NP_110434.3

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