Product Details

SNP ID

rs11643696

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:54926407 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACTTTTAATATTAAAGAAAAACATA[C/T]ACACTTCTTACATACACACTGATAG

Phenotype

MIM: 615624 MIM: 606195

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CRNDE PubMed Links

Additional Information

For this assay, SNP(s) [rs111640757] 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

CRNDE

Gene Name

colorectal neoplasia differentially expressed (non-protein coding)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001308963.1		Intron			NP_001295892.1
XM_017023562.1		Intron			XP_016879051.1
XM_017023563.1		Intron			XP_016879052.1

Gene

IRX5

Gene Name

iroquois homeobox 5

There are no transcripts associated with this gene.

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