Product Details

SNP ID

rs3127594

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:160217072 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTCCCAACTTTACTGTTTTTCACAC[A/T]TTTTTCTATTTTGTTTGCCTAGCCC

Phenotype

MIM: 602608

Polymorphism

A/T, Transversion 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	2202	UTR 3			NP_003049.2

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