Product Details

SNP ID
rs7217037
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:40066938 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGAGGAAAAATGTTTTTAAAAGTGC[C/T]TAGTTCATAACAAACTGTATATGTG
Phenotype
MIM: 190120
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
THRA PubMed Links
Additional Information
For this assay, SNP(s) [rs141197510] 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
THRA
Gene Name
thyroid hormone receptor, alpha
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001190918.1 Intron NP_001177847.1
NM_001190919.1 Intron NP_001177848.1
NM_003250.5 Intron NP_003241.2
NM_199334.3 Intron NP_955366.1

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