Product Details

SNP ID: rs2072242
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:14301093 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GCTCTCTTCCTGCGCAGTTCGCCTC[C/T]GCAGCCTCTGCGGGGAAGTGCCGGG
Phenotype: MIM: 604058
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: HS3ST3B1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006041.2	44	UTR 5			NP_006032.1
XM_017025479.1	44	Intron			XP_016880968.1

There are no transcripts associated with this gene.