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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