Product Details
- SNP ID
-
rs142235457
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:97854760 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCTCCGCCTATGCGGCTGCCTACGC[A/G]GGCCCCGACGGCGCGTACCCGCAGG
- Phenotype
-
MIM: 602617
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
FOXE1
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs3021526] 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
- FOXE1
- Gene Name
- forkhead box E1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_004473.3 |
1506 |
Silent Mutation |
GCA,GCG |
A282A |
NP_004464.2 |
- Gene
- PTCSC2
- Gene Name
- papillary thyroid carcinoma susceptibility candidate 2 (non-protein coding)
There are no transcripts associated with this gene.
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