Product Details

SNP ID

rs76690622

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:103916164 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCACTTCATAATAACTGCCAATTA[A/T]GATAGAACTTATTTAATCAATAAAG

Phenotype

MIM: 604573

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

C14orf2 PubMed Links

Additional Information

For this assay, SNP(s) [rs199787171] 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

C14orf2

Gene Name

chromosome 14 open reading frame 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127393.1		Intron			NP_001120865.1
NM_004894.2		Intron			NP_004885.1

View Full Product Details