Product Details

SNP ID: rs6687324
Assay Type: Functionally tested
NCBI dbSNP Submissions: 41
Location: Chr.1:58486574 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TAATATTCACTAATCATCTCAACTT[C/G]TCATAGGTACTATGGATACAGCAGT
Phenotype
Polymorphism: C/G, Transversion 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		Intron			NP_660286.1