Product Details

SNP ID: rs117278015
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.18:57352906 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGCTGGGGCTGGTCATGCTCAGCGT[C/T]GCCCTGCTGATTTTATCGCTCATCA
Phenotype: MIM: 609478
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ST8SIA3 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015879.2	417	Silent Mutation	GTC,GTT	V20V	NP_056963.2