Product Details

SNP ID: rs28541616
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.19:5815375 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGTGTGTGTGTGCAAACACCAGCAC[A/G]TGGATATAACGTTTCACCACAAGTG
Phenotype: MIM: 602018
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: NRTN PubMed Links
Additional Information: For this assay, SNP(s) [rs139182799] 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
XM_011528041.2		Intron			XP_011526343.1