Product Details

SNP ID: rs6861507
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:173315935 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CAATGATTCCCCTCCCCACCCAACC[A/G]CCGGCATGGATCATGAAAGACTGGG
Phenotype: MIM: 603665
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: STC2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003714.2	4131	UTR 3			NP_003705.1