Product Details

SNP ID

rs11864124

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:84012797 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTCAGAGTGGAAGGGAAGGCCCTTG[C/G]AGGACCCGGTGTTACTGGCCCGGGC

Phenotype

MIM: 615585

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SLC38A8 PubMed Links

Gene Details

Gene

SLC38A8

Gene Name

solute carrier family 38 member 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080442.2		Intron			NP_001073911.1
XM_017022946.1		Intron			XP_016878435.1

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