Product Details

SNP ID: rs79309522
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:86619134 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAGTCCTCAAGACCATTCATTGCCT[A/C]GTGCTTAGTAAAGCCAGATTATTTC
Phenotype: MIM: 603774
Polymorphism: A/C, Transversion 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.