Product Details

SNP ID: rs762870842
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:111079060 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTGCCGCGGCGCGGGCCGGGGGCGA[C/T]GGGGATCGGGACGCCGGCTGCAGGG
Phenotype: MIM: 104210
Polymorphism: C/T, Transition 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	2029	Missense Mutation	ACG,ATG	T355M	NP_000672.3