Product Details

SNP ID: rs28362202
Assay Type: Functionally tested
NCBI dbSNP Submissions: 13
Location: Chr.1:55039812 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCACGGCCTCTAGGTCTCCTCGCCA[A/G]GACAGCAACCTCTCCCCTGGCCCTC
Phenotype: MIM: 607786
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: PCSK9 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_174936.3	337	UTR 5			NP_777596.2