Product Details

SNP ID: rs16902283
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:86620005 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TTTTAGAAAGTGGTCACTGTGCTCC[C/T]AGTTTTTAAATTGGCTTACAATACT
Phenotype: MIM: 603774
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: COX7C PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001867.2		Intron			NP_001858.1

There are no transcripts associated with this gene.