Product Details

SNP ID

rs9378788

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:393362 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACAACCGCGAGGAGGACGCCGCGCT[C/G]TTCAAGGTCTCCGGCCTCGGGAGCC

Phenotype

MIM: 601900

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

IRF4 PubMed Links

Additional Information

For this assay, SNP(s) [rs74746812] 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

IRF4

Gene Name

interferon regulatory factor 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001195286.1	336	Silent Mutation	CTC,CTG	L70L	NP_001182215.1
NM_002460.3	336	Silent Mutation	CTC,CTG	L70L	NP_002451.2
XM_006715090.2	336	Silent Mutation	CTC,CTG	L70L	XP_006715153.1

View Full Product Details