Product Details

SNP ID: rs2404561
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.3:161497767 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGAGGCAATACTGTGTCATTGCCCA[A/G]TGATTTTCTCCATTGAACACCATGG
Phenotype
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: OTOL1 PubMed Links
Additional Information: For this assay, SNP(s) [rs5853936] 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_001080440.1		Intron			NP_001073909.1