Product Details

SNP ID
rs74639819
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:155926070 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TATAGAAGAAACGGAATCTGCAATA[C/T]CTAAGGGAAAAAAAAGGAATTATTA
Phenotype
MIM: 600550 MIM: 191070
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
CTSO PubMed Links
Additional Information
For this assay, SNP(s) [rs1543108] 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

Gene
CTSO
Gene Name
cathepsin O
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001334.2 981 Missense Mutation GAT,GGT D311G NP_001325.1
Gene
TDO2
Gene Name
tryptophan 2,3-dioxygenase
There are no transcripts associated with this gene.

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