Product Details

SNP ID: rs4656125
Assay Type: Functionally tested
NCBI dbSNP Submissions: 41
Location: Chr.1:86921332 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGCTTCATGTATTTTGAAGTGCTGT[A/G]ATTAAGTATATGCACATTTAGGCTG
Phenotype: MIM: 604844 MIM: 606254
Polymorphism: A/G, Transition 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

There are no transcripts associated with this gene.