Product Details

SNP ID: rs1110657
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.17:56794326 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GATTATATCTTGTCCTGCTTGGTCC[A/C]CAAAACTTACAGAGGAGAAATGAAA
Phenotype
Polymorphism: A/C, Transversion Substitution
Allele Nomenclature
Literature Links: C17orf67 PubMed Links
Additional Information: For this assay, SNP(s) [rs75088376] 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_001085430.2		Intron			NP_001078899.2
XM_011524735.2		Intron			XP_011523037.1