Product Details

SNP ID: rs1562394
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.2:29062576 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ATTCCGGACCCTTCCTGCGTGTTCT[C/G]CATGATACTGACCCCTTCTGTGGTG
Phenotype: MIM: 613425
Polymorphism: C/G, Transversion Substitution
Allele Nomenclature
Literature Links: C2orf71 PubMed Links
Additional Information: For this assay, SNP(s) [rs115478100] are located under a probe 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_001029883.2	6160	UTR 3			NP_001025054.1