Product Details

SNP ID
rs5398
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.3:170998041 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
TGGTTTCTGGAACTTTAAAAAATGT[A/G]AACAGGGTAAAGGCCAGGAGCACTC
Phenotype
MIM: 138160
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC2A2 PubMed Links

Gene Details

Gene
SLC2A2
Gene Name
solute carrier family 2 member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000340.1 1746 Silent Mutation NP_000331.1
NM_001278658.1 1746 Silent Mutation NP_001265587.1
NM_001278659.1 1746 Silent Mutation NP_001265588.1
XM_011513087.2 1746 Missense Mutation XP_011511389.1
XM_011513089.2 1746 Silent Mutation XP_011511391.1

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