Product Details

SNP ID: rs114939551
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.9:90612659 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAACACATCCCCTCAGGGTAGCAAG[C/G]CTCCTAACAGGCCAGGTGGGAATTA
Phenotype: MIM: 607863
Polymorphism: C/G, Transversion Substitution
Allele Nomenclature
Literature Links: DIRAS2 PubMed Links
Additional Information: For this assay, SNP(s) [rs75865905] 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_017594.4	1559	UTR 3			NP_060064.2