Product Details
- SNP ID
-
rs41268474
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
44
- Location
-
Chr.1:152720036 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCTCCCTGTTCCACCAGCTACTGCT[A/G]TCTGGCTCCCCGGACCTTCGGGGTG
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
C1orf68
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs59194678] 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
- C1orf68
- Gene Name
- chromosome 1 open reading frame 68
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001024679.2 |
515 |
Missense Mutation |
TAT,TGT |
Y172C |
NP_001019850.1 |
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