Product Details

SNP ID: rs187227683
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.20:45512795 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCGTCATGTAGGTTTGACAAGGGCC[C/T]TTTTCCATAGGAAAAGCGCATACAT
Phenotype: MIM: 613941
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: SPINT3 PubMed Links
Additional Information: For this assay, SNP(s) [rs16990288] are located under a primer 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_006652.1	142	Silent Mutation			NP_006643.1