Product Details

SNP ID

rs12047015

Assay Type

Functionally tested

NCBI dbSNP Submissions

38

Location

Chr.1:9001323 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTGGGGTGGTGGCAGGAAACCCACG[C/T]TATGACAATACGGTTCCAGCCTTAT

Phenotype

MIM: 610371

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC2A7 PubMed Links

Gene Details

Gene

SLC2A7

Gene Name

solute carrier family 2 member 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_207420.2		Intron			NP_997303.2
XM_011540824.2		Intron			XP_011539126.1
XM_011540825.2		Intron			XP_011539127.1

View Full Product Details