Product Details

SNP ID: rs12694382
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.2:216036433 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAGAGGGAGGCTCTTGCCAGGGGAC[A/G]TAAGGTCCCAGTGAGCTACAAACTA
Phenotype: MIM: 605843
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: PECR PubMed Links
Additional Information: For this assay, SNP(s) [rs78303896] 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_018441.5		Intron			NP_060911.2
XM_011511478.2		Intron			XP_011509780.1