Product Details

SNP ID: rs7349885
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.6:11555362 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CACGCATTTCACTATGATGTGTCTA[A/G]GTATGTGTGTGCGTGGTTTATTTTT
Phenotype
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: TMEM170B PubMed Links
Additional Information: For this assay, SNP(s) [rs74290142] 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_001100829.2		Intron			NP_001094299.1