Product Details

SNP ID: rs4985526
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.16:70388328 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: CTAGAAGACTCTGCCCAAGATGGTC[C/T]TGTCACCCATATTCTACCCAGGCCA
Phenotype: MIM: 607188
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ST3GAL2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006927.3		Intron			NP_008858.1