Product Details
- SNP ID
-
rs143532175
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.12:108517184 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGCAAACCGGACAGGGCGCAGCATG[C/G]CGCCACCAAGTGCACCAGCCCGTCC
- Phenotype
-
MIM: 611684
- Polymorphism
- C/G, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
FICD
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs2303634] 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
- FICD
- Gene Name
- FIC domain containing
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_007076.2 |
358 |
Missense Mutation |
GCC,GGC |
A71G |
NP_009007.2 |
- Gene
- SART3
- Gene Name
- squamous cell carcinoma antigen recognized by T-cells 3
There are no transcripts associated with this gene.
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