Product Details

SNP ID
rs200020721
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:73424560 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTCCAGTTATGATCTATTTAAATC[C/T]CGCCGTCCACTTTCTCTTCTAATTG
Phenotype
MIM: 614773
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
MSS51 PubMed Links
Additional Information
For this assay, SNP(s) [rs61738877] 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
MSS51
Gene Name
MSS51 mitochondrial translational activator
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001024593.1 1442 Missense Mutation GAG,GGG E459G NP_001019764.1

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