Product Details

SNP ID

rs13266400

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:116938377 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCGGGGACGGCAGGAGCACGGACA[G/T]CCAGGAGGAGGCCCTCGCCGCCAGC

Phenotype

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

AARD PubMed Links

Additional Information

For this assay, SNP(s) [rs76753109] 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

AARD

Gene Name

alanine and arginine rich domain containing protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001025357.2	153	Missense Mutation	AGC,ATC	S45I	NP_001020528.1
XM_011517043.2	153	Missense Mutation	AGC,ATC	S45I	XP_011515345.1

View Full Product Details