Product Details

SNP ID

rs17063109

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:133891432 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCGGCTTGCCCGGGGCTTCCTGCA[C/T]TGAGTCTCACAAGGAACCCAGTATA

Phenotype

MIM: 616058 MIM: 603306

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

TARID PubMed Links

Additional Information

For this assay, SNP(s) [rs4896010] 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

TARID

Gene Name

TCF21 antisense RNA inducing promoter demethylation

There are no transcripts associated with this gene.

Gene

TCF21

Gene Name

transcription factor 21

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003206.3		Intron			NP_003197.2
NM_198392.2		Intron			NP_938206.1

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