Product Details

SNP ID

rs516536

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:63369029 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATGTGGTGATTAAAATGCTCTGTAA[C/T]GATATAGTAGTGATGATTGCACAAC

Phenotype

MIM: 607579

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC22A9 PubMed Links

Gene Details

Gene

SLC22A9

Gene Name

solute carrier family 22 member 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_080866.2	159	Intron			NP_543142.2
XM_017017159.1	159	UTR 5			XP_016872648.1
XM_017017160.1	159	Intron			XP_016872649.1

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