Product Details

SNP ID: rs2966230
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:25696105 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGAACGTGTGCATCAGATTTTCAGG[C/G]CAAGATAGACTAATGGATTGGGATG
Phenotype: MIM: 604059
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: HS3ST4 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006040.2		Intron			NP_006031.2