Product Details

SNP ID: rs2236750
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:73166468 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AGGGGGGCGGGGGGGGCAGGTGCGT[A/G]AGACCATTCTCACCCTCCTCTCTAC
Phenotype: MIM: 182452
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: SSTR2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001050.2		Intron			NP_001041.1