Product Details

SNP ID
rs201128618
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:107792656 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGGTCTCCTGGAGGTTCTCCTCCA[G/T]CTTCAGCCCCAGGTTGTCAATCCCA
Phenotype
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
SLC35F2 PubMed Links

Gene Details

Gene
SLC35F2
Gene Name
solute carrier family 35 member F2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_017515.4 1505 Missense Mutation ATG,CTG M362L NP_059985.2

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