Product Details
- SNP ID
-
rs138969504
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:60703417 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CATTGGCCTGGCTCACATCGGCCTC[A/G]GCTCCATCATGGCGACGGTTCTCGT
- Phenotype
-
MIM: 606549
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
MS4A8
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs35956659] 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
- MS4A8
- Gene Name
- membrane spanning 4-domains A8
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_031457.1 |
462 |
Missense Mutation |
AGC,GGC |
S87G |
NP_113645.1 |
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