Product Details
- SNP ID
-
rs185242872
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:1270733 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCGGAGGAGCCGGCGGGCAGGAGGC[A/G]CGCGCGGCCGGTGCGGTCCAAGGCG
- Phenotype
-
MIM: 615416
MIM: 612211
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
BHLHA9
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs3951819] 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
- BHLHA9
- Gene Name
- basic helix-loop-helix family member a9
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001164405.1 |
170 |
Missense Mutation |
CAC,CGC |
H57R |
NP_001157877.1 |
- Gene
- TUSC5
- Gene Name
- tumor suppressor candidate 5
There are no transcripts associated with this gene.
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