Product Details

SNP ID

rs2465582

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:46769106 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAAATGACCTATAAGGTGGCTCCCA[A/G]TGTCAGTTAGGAGGAAGAGACAGTG

Phenotype

MIM: 608065

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC38A4 PubMed Links

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		Intron			NP_001137296.1
NM_018018.4		Intron			NP_060488.2
XM_005268997.2		Intron			XP_005269054.1

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