Product Details

SNP ID

rs3127592

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:160216812 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCTTCTCAAGGTCTTTTGTAGAAAA[C/T]ACACATTCATGCTTACCCAATCTAA

Phenotype

MIM: 602608

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC22A2 PubMed Links

Gene Details

Gene

SLC22A2

Gene Name

solute carrier family 22 member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003058.3	2462	UTR 3			NP_003049.2

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