Product Details

SNP ID: rs1800038
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:111079134 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGCCAAGGCGTCGCGCTGGCGCGGG[A/C]GGCAGAACCGCGAGAAGCGCTTCAC
Phenotype: MIM: 104210
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: ADRA2A PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000681.3	2103	Silent Mutation	AGG,CGG	R380R	NP_000672.3