Product Details
- SNP ID
-
rs201139614
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:124447586 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGGGAAAGTCTGGAAGTGCAGAGCG[A/C]CGGTGCCGGGAGGGCCAGGACTGCC
- Phenotype
-
- Polymorphism
- A/C, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
NKX1-2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs7089970] 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
- NKX1-2
- Gene Name
- NK1 homeobox 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001146340.1 |
814 |
Missense Mutation |
GGC,GTC |
G259V |
NP_001139812.1 |
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