Product Details

SNP ID: rs28385704
Assay Type: Functionally tested
NCBI dbSNP Submissions: 20
Location: Chr.1:55040430 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGGGTGAAGGAGTGAATGCCTGGAA[C/G]GTACTGGGAACTGCACCAGGCACAG
Phenotype: MIM: 607786
Polymorphism: C/G, Transversion 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		Intron			NP_777596.2