Product Details

SNP ID

rs7940321

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:64556648 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGGCATCTGGACATTCGCCAGCCTC[A/G]CCTGGTCCCGGCCCTACTGACCCAT

Phenotype

MIM: 607097

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC22A11 PubMed Links

Gene Details

Gene

SLC22A11

Gene Name

solute carrier family 22 member 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001307985.1		Intron			NP_001294914.1
NM_018484.3		Intron			NP_060954.1
XM_011545167.1		Intron			XP_011543469.1

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