Product Details
- SNP ID
-
rs200746821
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.16:1999507 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCCAGCACGCGTACCTGGGGGCGGC[A/G]GCATCCGGGGTGGGCAGGGGCCGCC
- Phenotype
-
MIM: 603927
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
SYNGR3
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs2286469] 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
- SYNGR3
- Gene Name
- synaptogyrin 3
There are no transcripts associated with this gene.
- Gene
- ZNF598
- Gene Name
- zinc finger protein 598
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_178167.3 |
2116 |
Missense Mutation |
CCG,CTG |
P681L |
NP_835461.2 |
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