Product Details
- SNP ID
-
rs11807924
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
37
- Location
-
Chr.1:203084535 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TGGGCCTTGGAGTCAGCAGGTCCCT[A/G]GAGAGACCCAAGGGAAGAGGACCGG
- Phenotype
-
MIM: 159980
MIM: 603145
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
MYOG
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs74570638] 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
- MYOG
- Gene Name
- myogenin (myogenic factor 4)
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_002479.5 |
|
Intron |
|
|
NP_002470.2 |
- Gene
- PPFIA4
- Gene Name
- PTPRF interacting protein alpha 4
There are no transcripts associated with this gene.
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