Product Details

SNP ID
rs148547690
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:1576642 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGGACCCATCATGGCCAGAAACAG[C/T]GGCTGCTGCAGAAGGGCGAAGAGCG
Phenotype
MIM: 610791
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC43A2 PubMed Links

Gene Details

Gene
SLC43A2
Gene Name
solute carrier family 43 member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001284498.1 1642 Silent Mutation CCA,CCG P505P NP_001271427.1
NM_001284499.1 1642 Silent Mutation CCA,CCG P364P NP_001271428.1
NM_001321364.1 1642 Silent Mutation CCA,CCG P505P NP_001308293.1
NM_001321365.1 1642 Silent Mutation CCA,CCG P505P NP_001308294.1
NM_152346.2 1642 Silent Mutation CCA,CCG P501P NP_689559.1
XM_017024177.1 1642 Silent Mutation CCA,CCG P501P XP_016879666.1
XM_017024178.1 1642 Silent Mutation CCA,CCG P501P XP_016879667.1
XM_017024179.1 1642 Silent Mutation CCA,CCG P468P XP_016879668.1

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