Product Details
- SNP ID
-
rs200546106
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
11
- Location
-
Chr.1:19814481 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGCAGAAGAGAGTCCTGGAGGAGGG[C/T]CAGCAGCTGCCCCGGGTGCTGGGGA
- Phenotype
-
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
RNF186
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs35541730] 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
- RNF186
- Gene Name
- ring finger protein 186
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_019062.1 |
798 |
Nonsense Mutation |
TGA,TGG |
*207W |
NP_061935.1 |
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