Product Details

SNP ID

rs10860582

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:100357174 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCAGCCAGACACCCCTTGGACTCTT[C/T]TTTGGAGGGGTGGGGAGCAGAGAGA

Phenotype

MIM: 607557

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC17A8 PubMed Links

Gene Details

Gene

SLC17A8

Gene Name

solute carrier family 17 member 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145288.1	96	UTR 5			NP_001138760.1
NM_139319.2	96	UTR 5			NP_647480.1

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