Product Details

SNP ID: rs12149938
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:25695771 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ATGCTATCTGGGATCTATTTGACTG[A/G]TTAGAGATCCACAGGTTAATTAAAG
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