Product Details
- SNP ID
-
rs182633028
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:10606925 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AATCTAAGTCATCTTGGCCAAAGCC[A/G]TCTGCCCTGCCCACTGCCTCAGTGG
- Phenotype
-
MIM: 608581
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
RP1L1
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs143284016] 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
- RP1L1
- Gene Name
- retinitis pigmentosa 1-like 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_178857.5 |
7402 |
Silent Mutation |
GAC,GAT |
D2391D |
NP_849188.4 |
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