Product Details

SNP ID

rs13436644

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:36607999 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTGGACATTTACTGATTGTGTACGT[C/T]GTGCAAGGCATCAGCTGGGTTCTGC

Phenotype

MIM: 600111

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC1A3 PubMed Links

Additional Information

For this assay, SNP(s) [rs147088440] 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

SLC1A3

Gene Name

solute carrier family 1 member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001166695.2		Intron			NP_001160167.1
NM_001166696.2		Intron			NP_001160168.1
NM_001289939.1		Intron			NP_001276868.1
NM_001289940.1		Intron			NP_001276869.1
NM_004172.4		Intron			NP_004163.3
XM_005248342.2		Intron			XP_005248399.1
XM_011514084.2		Intron			XP_011512386.1

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