Product Details

SNP ID

rs202114931

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:86214413 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTTAAGAGTTTGCACTTCCGACAT[C/T]TATTCCTCAGACACATCAGGGAGGC

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC7A13 PubMed Links

Additional Information

For this assay, SNP(s) [rs9693999] are located under a probe and SNP(s) [rs9656982] 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

SLC7A13

Gene Name

solute carrier family 7 member 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_138817.2	1489	Silent Mutation	TAA,TAG	*471*	NP_620172.2
XM_011516867.1	1489	Silent Mutation	TAA,TAG	*462*	XP_011515169.1

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