Product Details

SNP ID

rs970718

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.17:56798162 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CTAAGCAGCCTAACTCCTGTGAATG[C/T]TCCTGAATCCCTTCTACCCAGCCCG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C17orf67 PubMed Links

Additional Information

For this assay, SNP(s) [rs73323062] 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

C17orf67

Gene Name

chromosome 17 open reading frame 67

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001085430.2		Intron			NP_001078899.2
XM_011524735.2		Intron			XP_011523037.1

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