Product Details

SNP ID
rs200729611
Assay Type
Functionally Tested
NCBI dbSNP Submissions
5
Location
Chr.1:246544549 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGTGGTCTATTACAGTGGCGCTGC[A/G]CCTCCCAAAACAGTGCTTTAACAAG
Phenotype
MIM: 607055
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
TFB2M PubMed Links
Additional Information
For this assay, SNP(s) [rs3129568] are located under a probe and SNP(s) [rs3124119] 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
TFB2M
Gene Name
transcription factor B2, mitochondrial
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_022366.2 Intron NP_071761.1
XM_011544248.2 Intron XP_011542550.1
XM_017002055.1 Intron XP_016857544.1

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