Product Details

SNP ID: rs4662783
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:128272674 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGGGGGCCAGAGACAGGGAGGAGAG[A/G]AGAGGGCTCGATTTTCTGGGTCCAG
Phenotype: MIM: 604846
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: HS6ST1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004807.2		Intron			NP_004798.3