Product Details

SNP ID
rs143154754
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:71322866 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCACTGCTTGAGAAGCTGCTGGAC[C/T]GCCCGCCCCCTGGCCTGCAGAGGCC
Phenotype
MIM: 612373
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SLC29A3 PubMed Links

Gene Details

Gene
SLC29A3
Gene Name
solute carrier family 29 member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001174098.1 169 Missense Mutation CGC,TGC R38C NP_001167569.1
NM_018344.5 169 Missense Mutation CGC,TGC R38C NP_060814.4
XM_006717910.3 169 UTR 5 XP_006717973.1
XM_017016377.1 169 UTR 5 XP_016871866.1
XM_017016378.1 169 UTR 5 XP_016871867.1

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