Product Details

SNP ID
rs11183605
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:46765185 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCTTTACTAAAATATAAAATACACA[A/G]GTGATCTTACTATGATTTGAAAAAA
Phenotype
MIM: 608065
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SLC38A4 PubMed Links
Additional Information
For this assay, SNP(s) [rs55642677] 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
SLC38A4
Gene Name
solute carrier family 38 member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001143824.1 3559 UTR 3 NP_001137296.1
NM_018018.4 3559 UTR 3 NP_060488.2
XM_005268997.2 3559 UTR 3 XP_005269054.1

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