Product Details

SNP ID
rs11556559
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:104128437 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCTTGCTTACCATCATGAGGCTG[T/C]ATAACATAATGACTTCCTCCAATAT
Phenotype
MIM: 189904
Polymorphism
T/C, Transition Substitution
Allele Nomenclature
Literature Links
NFYB PubMed Links
Additional Information
For this assay, SNP(s) [rs145973669] 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
NFYB
Gene Name
nuclear transcription factor Y subunit beta
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006166.3 1007 Missense Mutation ATA,ATG I29M NP_006157.1
XM_005268908.4 1007 Missense Mutation ATA,ATG I30M XP_005268965.1
XM_005268909.4 1007 Missense Mutation ATA,ATG I30M XP_005268966.1
XM_005268910.4 1007 Missense Mutation ATA,ATG I30M XP_005268967.1

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