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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