Product Details

SNP ID

rs150052319

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:99513164 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGGCTAGAAATGTAAGCTGCTTTC[C/T]AGTCAGGCACACCCCTCATCCCAGA

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C4orf17 PubMed Links

Additional Information

For this assay, SNP(s) [rs554111966] 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

C4orf17

Gene Name

chromosome 4 open reading frame 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032149.2	445	Missense Mutation	CCA,CTA	P28L	NP_115525.2
XM_011532315.1	445	Missense Mutation	CCA,CTA	P28L	XP_011530617.1

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