Product Details

SNP ID
rs150523975
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:227688276 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGATTCCAAATACCAAGGCATAGC[A/G]TTCCACATTCAGATTAACTGCAATC
Phenotype
MIM: 606152
Polymorphism
A/G, Transition 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 1370 Missense Mutation NP_079519.1
XM_005246874.3 1370 Missense Mutation XP_005246931.1
XM_011511931.2 1370 Missense Mutation XP_011510233.1
XM_011511932.1 1370 Missense Mutation XP_011510234.1
XM_011511933.1 1370 Missense Mutation XP_011510235.1
XM_017005030.1 1370 Missense Mutation XP_016860519.1
XM_017005031.1 1370 Missense Mutation XP_016860520.1
XM_017005032.1 1370 Missense Mutation XP_016860521.1
XM_017005033.1 1370 Missense Mutation XP_016860522.1
XM_017005034.1 1370 Missense Mutation XP_016860523.1

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