Product Details
- SNP ID
-
rs3187415
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:190056055 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TCACTTTATACAGCCATCATGAATC[C/G]ATAAGTGAATGTTAATCATGTAAAA
- Phenotype
-
MIM: 615117
MIM: 601788
- Polymorphism
- C/G, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
C2orf88
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs199602321] 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
- C2orf88
- Gene Name
- chromosome 2 open reading frame 88
- Gene
- MSTN
- Gene Name
- myostatin
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_005259.2 |
2464 |
UTR 3 |
|
|
NP_005250.1 |
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