Product Details

SNP ID
rs942379
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.6:25849392 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
ATTGTACCTGACTAAGAAGAAATCC[A/G]CTGACAGTGGGTACAATGACAGGTG
Phenotype
MIM: 611034
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SLC17A3 PubMed Links

Gene Details

Gene
SLC17A3
Gene Name
solute carrier family 17 member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001098486.1 1220 Silent Mutation AGC,AGT S448S NP_001091956.1
NM_006632.3 1220 Silent Mutation AGC,AGT S370S NP_006623.2

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