Product Details

SNP ID: rs1407132
Assay Type: Validated
NCBI dbSNP Submissions: 38
Location: Chr.1:86928231 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: AGGTGTGATGTAAAAGGACATTATC[G/T]TAAGTTTTCAGTGATAAAAAATATA
Phenotype: MIM: 604844
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: HS2ST1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001134492.1		Intron			NP_001127964.1
NM_012262.3		Intron			NP_036394.1