Product Details

SNP ID

rs2075437

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:109279642 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAGTTCTCTGCCCAAGCCGGGTGCC[A/G]GGGTTCCAGGGCAGGTGAGGCTGAC

Phenotype

MIM: 609429

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FOXN4 PubMed Links

Additional Information

For this assay, SNP(s) [rs80262509] 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

FOXN4

Gene Name

forkhead box N4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_213596.2	1877	UTR 3			NP_998761.2
XM_011537922.2	1877	UTR 3			XP_011536224.1
XM_011537923.2	1877	Intron			XP_011536225.1
XM_017018818.1	1877	UTR 3			XP_016874307.1
XM_017018819.1	1877	Intron			XP_016874308.1

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