Product Details

SNP ID: rs138421941
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.2:21001973 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGTAATCAGAAATTATTTTCTTCGT[C/T]GCAATGGCCTGGCTTTTAATTATTT
Phenotype: MIM: 107730
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: APOB PubMed Links
Additional Information: For this assay, SNP(s) [rs12713450] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000384.2	13577	Silent Mutation	GCA,GCG	A4483A	NP_000375.2