Product Details

SNP ID: rs9922960
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:25701858 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GGATTTATTCTAAGAATGGAAGGAT[A/G]GTTCAATCTTGGGGAATGTAATAAT
Phenotype: MIM: 604059
Polymorphism: A/G, Transition 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