Product Details

SNP ID: rs72889606
Assay Type: Functionally tested
NCBI dbSNP Submissions: 16
Location: Chr.1:28819637 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGTTCTCATTTGCAAATGGGGACAA[A/G]AAGGCTCAGAGGGAGCGAGTGCCTC
Phenotype: MIM: 165195
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: OPRD1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000911.3		Intron			NP_000902.3