Product Details
- SNP ID
-
rs143284297
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:32440004 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GATTTTTCATCATAGCTGTGCTGAT[G/T]AGCGCTCAGGAATCATGGGCTATCA
- Phenotype
-
MIM: 142860
- Polymorphism
- G/T, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
HLA-DRA
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs16822586] 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
- HLA-DRA
- Gene Name
- major histocompatibility complex, class II, DR alpha
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_019111.4 |
163 |
Missense Mutation |
ATG,ATT |
M18I |
NP_061984.2 |
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