Product Details

SNP ID

rs183247983

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:52439353 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGGATGTTATCTGAGAGGCGACAG[A/G]GGAGTGCTGCCGAGGAGAAGGCTGA

Phenotype

MIM: 611416

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TOX3 PubMed Links

Additional Information

For this assay, SNP(s) [rs9925256] 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

TOX3

Gene Name

TOX high mobility group box family member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080430.3	1850	Missense Mutation	CCT,TCT	P535S	NP_001073899.2
NM_001146188.2	1850	Missense Mutation	CCT,TCT	P530S	NP_001139660.1
XM_005255892.3	1850	Missense Mutation	CCT,TCT	P534S	XP_005255949.1
XM_011523002.2	1850	Missense Mutation	CCT,TCT	P512S	XP_011521304.1
XM_017023142.1	1850	Missense Mutation	CCT,TCT	P531S	XP_016878631.1

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