Product Details

SNP ID
rs12105323
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:227685657 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CATACCCCTACCCTCAAATTAACCT[C/G]TCACTTCAGCCTCCCAAAATGCTGG
Phenotype
MIM: 606152
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SLC19A3 PubMed Links

Gene Details

Gene
SLC19A3
Gene Name
solute carrier family 19 member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_025243.3 3397 UTR 3 NP_079519.1
XM_005246874.3 3397 UTR 3 XP_005246931.1
XM_011511931.2 3397 UTR 3 XP_011510233.1
XM_011511932.1 3397 UTR 3 XP_011510234.1
XM_011511933.1 3397 UTR 3 XP_011510235.1
XM_017005030.1 3397 UTR 3 XP_016860519.1
XM_017005031.1 3397 UTR 3 XP_016860520.1
XM_017005032.1 3397 UTR 3 XP_016860521.1
XM_017005033.1 3397 UTR 3 XP_016860522.1
XM_017005034.1 3397 UTR 3 XP_016860523.1

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