Product Details

SNP ID
rs188774288
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:25914622 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGTGGCAGTGGAAGAGATGATTCC[C/T]GCGATGAGCCCAAATCCCCTTGAGA
Phenotype
MIM: 611049
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC17A2 PubMed Links

Gene Details

Gene
SLC17A2
Gene Name
solute carrier family 17 member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286123.1 1645 Silent Mutation GCA,GCG A420A NP_001273052.1
NM_001286125.1 1645 Missense Mutation CAG,CGG Q371R NP_001273054.1
NM_005835.3 1645 Missense Mutation CAG,CGG Q371R NP_005826.1
XM_005248784.2 1645 Silent Mutation GCA,GCG A420A XP_005248841.1
XM_006714949.3 1645 Silent Mutation GCA,GCG A420A XP_006715012.1
XM_006714950.2 1645 Silent Mutation GCA,GCG A397A XP_006715013.1
XM_006714951.1 1645 Missense Mutation CAG,CGG Q371R XP_006715014.1
XM_017010159.1 1645 Silent Mutation GCA,GCG A397A XP_016865648.1
XM_017010160.1 1645 Intron XP_016865649.1

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