Product Details

SNP ID
rs13306766
Assay Type
Functionally tested
NCBI dbSNP Submissions
14
Location
Chr.1:9037597 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTCCTCTCCAGAGTCACTGTTCCG[A/T]AGTGACAGGTGGAAGCTCTTTCAGT
Phenotype
MIM: 138230
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
SLC2A5 PubMed Links

Gene Details

Gene
SLC2A5
Gene Name
solute carrier family 2 member 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001135585.1 1716 Intron NP_001129057.1
NM_003039.2 1716 Missense Mutation ACG,TCG T499S NP_003030.1
XM_005263491.3 1716 Missense Mutation ACG,TCG T499S XP_005263548.1
XM_017002133.1 1716 Missense Mutation ACG,TCG T499S XP_016857622.1
XM_017002134.1 1716 Missense Mutation ACG,TCG T499S XP_016857623.1
XM_017002135.1 1716 Missense Mutation ACG,TCG T499S XP_016857624.1
XM_017002136.1 1716 Missense Mutation ACG,TCG T499S XP_016857625.1
XM_017002137.1 1716 Missense Mutation ACG,TCG T499S XP_016857626.1
XM_017002138.1 1716 Missense Mutation ACG,TCG T499S XP_016857627.1
XM_017002139.1 1716 Missense Mutation ACG,TCG T499S XP_016857628.1
XM_017002140.1 1716 Missense Mutation ACG,TCG T499S XP_016857629.1
XM_017002141.1 1716 Missense Mutation ACG,TCG T499S XP_016857630.1
XM_017002142.1 1716 Missense Mutation ACG,TCG T440S XP_016857631.1

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