Product Details

SNP ID: rs658202
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.17:39162988 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCCACCCAGGTTCACCAAACACCTG[C/T]TCGGAGCCAGGCCCCGTGCTGGGCC
Phenotype
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: ARL5C PubMed Links
Additional Information: For this assay, SNP(s) [rs75717602,rs76651321] 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_001143968.1		Intron			NP_001137440.1