Product Details
- SNP ID
-
rs200064109
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.16:1486134 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TCCCCACGAAGGCCTCGGAGCTGTC[A/G]AATCCGCCCCCCACGCTGTCTTGTT
- Phenotype
-
MIM: 613442
MIM: 611140
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
PTX4
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs114122805,rs79505704] 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
- PTX4
- Gene Name
- pentraxin 4
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001013658.1 |
1227 |
Silent Mutation |
TTC,TTT |
F409F |
NP_001013680.1 |
- Gene
- TELO2
- Gene Name
- telomere maintenance 2
There are no transcripts associated with this gene.
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