Product Details
- SNP ID
-
rs200731541
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:133928593 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGGTGTGGCGCGGCCCACTCAGGAG[C/T]CCCTTCCAGTGTAGACTCCAGGAGG
- Phenotype
-
MIM: 601460
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
C3orf36
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs76311816] 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
- C3orf36
- Gene Name
- chromosome 3 open reading frame 36
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_025041.2 |
1220 |
Missense Mutation |
ACT,GCT |
T71A |
NP_079317.2 |
- Gene
- SLCO2A1
- Gene Name
- solute carrier organic anion transporter family member 2A1
There are no transcripts associated with this gene.
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