Product Details

SNP ID
rs8187717
Assay Type
DME
NCBI dbSNP Submissions
NA
Location
Chr.6:160348765 on Build GRCh38
Set Membership
DME Validated Inventoried
Context Sequence [VIC/FAM]
TCTCAGCTGCGCGGACCCACTCGCC[G/T]CCTTCCCCAACCGCTCGGCTCCCCT
Phenotype
MIM: 604842
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
SLC22A3 PubMed Links

Gene Details

Gene
SLC22A3
Gene Name
solute carrier family 22 member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_021977.3 388 Missense Mutation GCC,TCC A116S NP_068812.1
XM_005267106.4 388 Intron XP_005267163.1
XM_005267107.3 388 Missense Mutation GCC,TCC A116S XP_005267164.1
XM_011536075.2 388 Intron XP_011534377.1
XM_011536076.2 388 Intron XP_011534378.1
XM_017011203.1 388 Intron XP_016866692.1

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