Product Details

SNP ID: rs139687018
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:25696774 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAGGAAAATGGTCAGTGCTCAGCAG[C/T]ATATTTTGCATGTGGCAACTGGGGA
Phenotype: MIM: 604059
Polymorphism: C/T, 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