Product Details

SNP ID: rs76177820
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.18:57355655 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TATTAATTTTATGGACAACCCAGAA[C/T]GTTTTCATGGGTAGAACACATTCTA
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		Intron			NP_056963.2