Product Details

SNP ID

rs140566193

Assay Type

Functionally Tested

NCBI dbSNP Submissions

11

Location

Chr.1:943917 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCCATCTCTCTGCAGGTGGCCAGG[C/T]GCCTGGGCCGAGTTTTCTACGTGGC

Phenotype

MIM: 610770 MIM: 616765

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NOC2L PubMed Links

Additional Information

For this assay, SNP(s) [rs115454328,rs7523549] 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

NOC2L

Gene Name

NOC2 like nucleolar associated transcriptional repressor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015658.3	1890	Intron			NP_056473.2

Gene

SAMD11

Gene Name

sterile alpha motif domain containing 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152486.2	1890	Missense Mutation	CGC,TGC	R604C	NP_689699.2

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