Product Details

SNP ID
rs146382802
Assay Type
Functionally tested
NCBI dbSNP Submissions
6
Location
Chr.1:9037709 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTATGAACGTCTTGGCCTTGGTCTC[C/T]GGGACAATCAAGAAGATGTAGATGG
Phenotype
MIM: 138230
Polymorphism
C/T, Transition 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 1604 Intron NP_001129057.1
NM_003039.2 1604 Silent Mutation CCA,CCG P461P NP_003030.1
XM_005263491.3 1604 Silent Mutation CCA,CCG P461P XP_005263548.1
XM_017002133.1 1604 Silent Mutation CCA,CCG P461P XP_016857622.1
XM_017002134.1 1604 Silent Mutation CCA,CCG P461P XP_016857623.1
XM_017002135.1 1604 Silent Mutation CCA,CCG P461P XP_016857624.1
XM_017002136.1 1604 Silent Mutation CCA,CCG P461P XP_016857625.1
XM_017002137.1 1604 Silent Mutation CCA,CCG P461P XP_016857626.1
XM_017002138.1 1604 Silent Mutation CCA,CCG P461P XP_016857627.1
XM_017002139.1 1604 Silent Mutation CCA,CCG P461P XP_016857628.1
XM_017002140.1 1604 Silent Mutation CCA,CCG P461P XP_016857629.1
XM_017002141.1 1604 Silent Mutation CCA,CCG P461P XP_016857630.1
XM_017002142.1 1604 Silent Mutation CCA,CCG P402P XP_016857631.1

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