Product Details

SNP ID: rs11068076
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.12:116567162 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGTTTTTGGAGATTTAGAGTGCTGA[A/G]AGATGCTGTTTGCACACCACCAAGA
Phenotype
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: MAP1LC3B2 PubMed Links
Additional Information: For this assay, SNP(s) [rs75471917] 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_001085481.1		Intron			NP_001078950.1
XM_011538652.2		Intron			XP_011536954.1