Product Details

SNP ID: rs7199655
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:70388360 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCATATTCTACCCAGGCCAGCAAGA[G/A]GCTCACAATCGGATCTGCCCCGTGG
Phenotype: MIM: 607188
Polymorphism: G/A, 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