Product Details

SNP ID: rs149689309
Assay Type: Functionally tested
NCBI dbSNP Submissions: 4
Location: Chr.1:58481035 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTCCTGTTTTTGAATAGGAAGAGTA[C/T]CCATTTTCTGTTTCTTCGTGATATT
Phenotype
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: OMA1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_145243.4	1618	Missense Mutation	GAT,GGT	D502G	NP_660286.1