Product Details

SNP ID: rs138797613
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:111078288 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCTGGCCTCGGCCGACATCCTGGTG[A/G]CCACGCTCGTCATCCCTTTCTCGCT
Phenotype: MIM: 104210
Polymorphism: A/G, 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	1257	Missense Mutation	ACC,GCC	T98A	NP_000672.3