Product Details

SNP ID

rs462469

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:132300818 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTTCCATCAGGCAGCAGTTGAGCA[C/G]GAACGCAAGCAGGGACTGGTGGGAC

Phenotype

MIM: 604190

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SLC22A4 PubMed Links

Gene Details

Gene

SLC22A4

Gene Name

solute carrier family 22 member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003059.2		Intron			NP_003050.2
XM_006714675.3		Intron			XP_006714738.1
XM_011543589.2		Intron			XP_011541891.1
XM_017009776.1		Intron			XP_016865265.1

View Full Product Details