Product Details

SNP ID
rs80074591
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:76329284 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTCTTTTCATCTGAAAACCCTAT[C/T]ATCTAGCAATAAGTTAAATTAGAGA
Phenotype
MIM: 605356
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
YWHAG PubMed Links
Additional Information
For this assay, SNP(s) [rs200070734] 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

Gene
YWHAG
Gene Name
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_012479.3 1254 UTR 3 NP_036611.2

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