Product Details

SNP ID: rs201733731
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:14301687 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTACTCGTGCGCCGGCTCCTGCGCC[G/T]CCGCGCCGGGGCTGCTGCTCCTGGG
Phenotype: MIM: 604058
Polymorphism: G/T, Transversion 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	638	Missense Mutation	GCC,TCC	A57S	NP_006032.1
XM_017025479.1	638	Intron			XP_016880968.1

There are no transcripts associated with this gene.