Product Details

SNP ID

rs186991229

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:43360360 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACCACATCGAATACCGAGATGTGC[C/G]AGGTGGGGCAGGTGTGTCAGGAGAC

Phenotype

MIM: 162860

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

CD177 PubMed Links

Additional Information

For this assay, SNP(s) [rs10425835] 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

CD177

Gene Name

CD177 molecule

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020406.3	771	Missense Mutation	CAG,GAG	Q239E	NP_065139.2
XM_017027021.1	771	Missense Mutation	CAG,GAG	Q239E	XP_016882510.1
XM_017027022.1	771	Missense Mutation	CAG,GAG	Q239E	XP_016882511.1

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