Product Details
- SNP ID
-
rs201283961
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:136984783 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACTTTGCCTTGCTGTACTTGGAGAT[G/T]CGGAAAGGGGGCCTGCGGAACCAGT
- Phenotype
-
MIM: 616315
MIM: 606533
MIM: 176803
- Polymorphism
- G/T, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
C9orf142
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs77874259] 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
- C9orf142
- Gene Name
- chromosome 9 open reading frame 142
There are no transcripts associated with this gene.
- Gene
- CLIC3
- Gene Name
- chloride intracellular channel 3
There are no transcripts associated with this gene.
- Gene
- LCNL1
- Gene Name
- lipocalin like 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_207510.3 |
861 |
Missense Mutation |
ATG,ATT |
M89I |
NP_997393.3 |
- Gene
- PTGDS
- Gene Name
- prostaglandin D2 synthase
There are no transcripts associated with this gene.
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