Product Details

SNP ID
rs428064
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:151316937 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGAAGCCCAGGATGCTGATCAGGGC[A/G]TCCTTGAAGATGGTGAGGGGGCTCA
Phenotype
MIM: 608331
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SLC36A2 PubMed Links
Additional Information
For this assay, SNP(s) [rs10042608] are located under a probe 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
SLC36A2
Gene Name
solute carrier family 36 member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_181776.2 1370 Silent Mutation GAC,GAT D444D NP_861441.2
XM_005268377.3 1370 Intron XP_005268434.1
XM_006714756.3 1370 Silent Mutation GAC,GAT D411D XP_006714819.1
XM_017009083.1 1370 Intron XP_016864572.1
XM_017009084.1 1370 Silent Mutation GAC,GAT D246D XP_016864573.1

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