Product Details
- SNP ID
-
rs148619520
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
13
- Location
-
Chr.1:168226097 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGGCCGCAATGGACAAGCTGAAGAA[C/G]GTGCTGAGCGGGCAGGACACGGAGG
- Phenotype
-
- Polymorphism
- C/G, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
SFT2D2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs138834549] 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
- SFT2D2
- Gene Name
- SFT2 domain containing 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_199344.2 |
81 |
Missense Mutation |
AAC,AAG |
N6K |
NP_955376.1 |
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