Product Details

SNP ID
rs200259642
Assay Type
Functionally Tested
NCBI dbSNP Submissions
6
Location
Chr.1:9003463 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGAATAACCACGTAGATGTAAATC[G/T]CAGTGAGGAGGCAGATTCCGGCAAA
Phenotype
MIM: 610371
Polymorphism
G/T, Transversion 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 1376 Missense Mutation NP_997303.2
XM_011540824.2 1376 Intron XP_011539126.1
XM_011540825.2 1376 Intron XP_011539127.1

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