Product Details
- SNP ID
-
rs12767604
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:99741756 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CATTTGTTTGTTTGTTTGTTTGGTA[A/G]AGATGGAGTCTCACCATTTTACCCA
- Phenotype
-
MIM: 603646
MIM: 610101
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
COX15
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs143080744] 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
- COX15
- Gene Name
- COX15, cytochrome c oxidase assembly homolog
There are no transcripts associated with this gene.
- Gene
- CUTC
- Gene Name
- cutC copper transporter
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_015960.2 |
|
Intron |
|
|
NP_057044.2 |
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